Qfitlia Injection, Solution
FDA Label NDC 58468-0348

Thrombotic Events

Serious thrombotic events have occurred in QFITLIA-treated patients with risk factors for thromboembolism including persistent antithrombin (AT) activity less than 15%, use of QFITLIA 80 mg once monthly, presence of indwelling venous catheters, and in the post-operative setting when bleed management guidelines were not followed.

Monitor AT activity using an FDA-cleared test and target AT activity 15–35% to reduce the risk of thrombosis. Monitor patients for signs and symptoms of thrombotic events. Interrupt QFITLIA in patients with a thrombotic event and manage as clinically indicated. (5.1)

Acute and Recurrent Gallbladder Disease

Acute and recurrent gallbladder disease, including cholelithiasis and cholecystitis have occurred in QFITLIA-treated patients, some of whom required cholecystectomy or had complications (e.g., pancreatitis) related to gallbladder disease. Monitor patients for signs and symptoms of acute and recurrent gallbladder disease.

Consider interruption or discontinuation of QFITLIA if gallbladder disease occurs. Consider alternative treatment for hemophilia in patients with a history of symptomatic gallbladder disease. (5.2)

Missed dose

If a dose of QFITLIA is missed, administer as soon as possible; thereafter, resume the patient's usual dosing schedule of either once every month or once every two months, as applicable, from the last dose.

Breakthrough Bleed Management

If breakthrough bleeding requiring on-demand treatment with CFC or BPA occurs during the first 7 days after QFITLIA initiation, manage the bleed using the patient's prior dosing regimen of CFC or BPA.

If breakthrough bleeding occurs after 7 days from the first QFITLIA dose, bleeds should be managed with a reduced dose and frequency of CFC/BPA to minimize the risk of thrombotic events. Initially, the weight-based dose of a CFC/BPA should be reduced, and the dosing interval doubled compared to the standard dose. This reduced dosing is shown in Table 2. If adequate hemostatic control is not achieved, higher doses may be used based on clinical judgement. Combination use of antifibrinolytics with CFC or BPA has not been studied.

Use of QFITLIA During Surgical Interventions

In clinical studies, patients with hemophilia A or B with or without inhibitors have undergone both major (N=60) and minor (N=71) surgical procedures without discontinuing QFITLIA prophylaxis. Utilize bleed management guidelines during the perioperative period for hemostatic management.

Clinically relevant adverse reactions in less than 5% of patients include:

• Dyspepsia
• Abdominal pain

Risk Summary

There are no available data on QFITLIA use in pregnant women to evaluate for a drug-associated risk of major birth defects, miscarriage, or other adverse maternal or fetal outcomes. Reproduction studies in pregnant animals have not been conducted with fitusiran. It is not known whether QFITLIA can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. QFITLIA should be used during pregnancy only if the potential benefit justifies the potential risks, including those to the fetus.

The estimated background risk of major birth defects and miscarriage for the indicated population is unknown. All pregnancies have a background risk of birth defect, loss, or other adverse outcomes. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2–4% and 15–20%, respectively.

Risk Summary

There are no data on the presence of fitusiran or its metabolite in human milk, the effects on the breastfed child, or the effects on milk production. It is not known whether QFITLIA is safe for use during breastfeeding. The developmental and health benefits of breastfeeding should be considered along with the mother's clinical need for QFITLIA and any potential adverse effects on the breastfed infant from QFITLIA or from the underlying maternal condition.

Contraception

Females

Use of QFITLIA in women using hormonal contraceptives may increase the risk of thrombotic events. Estrogen based hormonal contraceptives are an established risk factor for thrombosis in women with inherited AT deficiency. Advise patients using hormonal contraceptives to use an alternative non-hormonal contraception prior to starting treatment with and while receiving QFITLIA.

Specific Populations

QFITLIA has only been studied in male patients. The pharmacokinetics of fitusiran is not influenced by race. QFITLIA has not been studied in children <12 years old.

No clinical study to evaluate the effect of hepatic impairment or renal impairment on the pharmacokinetics of QFITLIA was conducted. In the pivotal studies, 12 patients had mild renal impairment (eGFR ≥60 to <90 mL/min/1.73 m²) and 1 patient had moderate renal impairment (eGFR 30 mL/min/1.73 m² to <60 mL/min/1.73 m²). Population PK analysis indicated no impact of renal impairment on the exposure (C_max and AUC) of QFITLIA in patients with mild renal impairment.

Drug Interaction Studies

Clinical Studies

No clinical drug-drug interaction studies have been conducted to evaluate the potential of QFITLIA to interact with other co-administered drugs which are either substrates, inhibitors or inducers of CYP isozymes, or are substrates or inhibitors of drug transporters.

In Vitro Studies

Results from in vitro studies evaluating the potential of co-administered drugs to increase the PK exposure of QFITLIA, and the potential of QFITLIA to increase the PK exposure of co-administered drugs, indicate that CYP- or transporter-mediated interactions between QFITLIA and co-administered drugs are unlikely at clinically relevant concentrations.

ATLAS-INH

ATLAS-INH was a randomized, multicenter, open-label clinical study in 57 adult and pediatric males (aged ≥12 years) with hemophilia A or B with inhibitory antibodies to factor VIII (FVIII) or factor IX (FIX), who previously received on-demand (episodic) treatment with BPAs for bleeding. Eligible patients were randomized in a 2:1 ratio to receive QFITLIA prophylaxis at a fixed dose 80 mg SC monthly (N=38) or BPA on-demand for treatment of breakthrough bleeding episodes (N=19) for 9 months. The 80 mg dose of QFITLIA is not approved because of an increased risk of serious thrombotic events, gallbladder events (including the need for cholecystectomy) and hepatotoxicity [see Boxed Warning and Warnings and Precautions (5.1, 5.2, 5.3)].

Of the 57 enrolled patients all had inhibitors; 45 patients had Hemophilia A and 12 had Hemophilia B. All patients in the study were male. The mean age of patients was 28.4 years, and 10 (17.5%) patients were 12–17 years of age. A total of 68.4% of patients were Asian, 28.1% were White, 1.8% were other, and 1.8% were multiple races; 5.3% patients identified as Hispanic or Latino and 94.7% identified as not Hispanic or Latino. Generally, the demographic and patient characteristics at baseline were comparable between the patients with hemophilia A and B.

ATLAS A/B

ATLAS A/B was a randomized, multicenter, open-label clinical study in 120 adult and pediatric males (aged ≥12 years) with hemophilia A or B without inhibitory antibodies to FVIII or FIX, who previously received on-demand (episodic) treatment with CFC for bleeding. Eligible patients were randomized in a 2:1 ratio to receive QFITLIA prophylaxis at a fixed dose of 80 mg SC monthly (N=80) or CFCs on-demand to treat breakthrough bleeding episodes (N=40) for 9 months. The 80 mg dose of QFITLIA is not approved because of an increased risk of serious thrombotic events, gallbladder events (including the need for cholecystectomy) and hepatotoxicity [see Boxed Warning and Warnings and Precautions (5.1, 5.2, 5.3)].

Of the 120 enrolled patients none had inhibitors; 93 patients had Hemophilia A and 27 had Hemophilia B. All patients in the study were male. The mean age of patients was 33.8 years, and 14 (11.7%) patients were 12–17 years of age. A total of 59.2% of patients were Asian, 37.5% were White, 1.7% were Black or African American, and 1.7% were multiple races; 3.3% of patients identified as Hispanic or Latino, 90.8% identified as not Hispanic or Latino, and 5.8% had ethnicity information unreported. Generally, the demographic and patient characteristics at baseline were comparable between the patients with hemophilia A and B.

ATLAS-OLE

A total of 227 patients rolled over from two clinical studies (ATLAS-INH and ATLAS-A/B) and ATLAS-PPX, a crossover study in patients previously on CFC or BPA prophylaxis, and were treated with QFITLIA in ATLAS-OLE. This multicenter open-label extension study evaluated the long-term safety and efficacy of QFITLIA in adult and pediatric males aged ≥12 years with hemophilia A or B, with or without inhibitory antibodies to FVIII or FIX. Eligible patients initially received QFITLIA 80 mg SC once monthly. The study was amended to evaluate the efficacy and safety of the AT-DR. A total of 213 patients were subsequently transitioned to AT-DR targeting AT activity of 15–35%.

In the AT-DR, the QFITLIA starting dose was 50 mg every two months, and dosing was individually adjusted based on AT activity level using the INNOVANCE Antithrombin assay. The dose could be increased to 50 mg every month or 80 mg every month or decreased to 20 mg every two months or 20 mg every month. QFITLIA was discontinued if AT activity was <15% at the lowest dose. No patients required escalation to 80 mg every month to achieve the target AT range. The dose required to maintain AT activity 15–35% in patients who initiated dosing on 50 mg every two months was: 50 mg every two months (35.8% of patients), 50 mg every month (15.7% of patients), 20 mg every two months (30.9% of patients), or 20 mg every month (2.9% of patients). A total of 14.7% of patients discontinued QFITLIA due to more than one AT activity <15%.

Patients with known co-existing coagulation disorders other than hemophilia A or B, increased risk of thrombosis as assessed by history of arterial or venous thromboembolism, significant valvular disease or atrial fibrillation, or co-existing thrombophilic disorder (e.g., Factor V Leiden mutation), AT activity <60% at screening, platelet count ≤100,000/μL, eGFR ≤45 mL/min (using the MDRD), or clinically significant liver disease were not eligible for enrollment.

The efficacy of QFITLIA AT-DR in ATLAS-OLE was evaluated for a duration of 7 months (primary efficacy period) following a 6-month dose adjustment period. The median observed annualized bleeding rate (IQR) for treated bleeds was 3.7 (0.0; 7.5) overall, 1.9 (0.0; 5.6) in inhibitor patients and 3.8 (0.0; 11.2) in non-inhibitor patients.

QFITLIA Prophylaxis Compared to On-Demand BPA or CFC

The efficacy results of QFITLIA prophylaxis using AT-DR in ATLAS-OLE compared to on-demand BPA or CFC control data from studies ATLAS-INH and ATLAS-A/B with respect to rate of treated bleeds, treated spontaneous bleeds, and treated joint bleeds are shown in Table 5 (patients with inhibitors) and Table 6 (patients without inhibitors) below.

Table 5: Annualized Bleed Rate for Treated Bleeds with QFITLIA Prophylaxis versus On-Demand BPA in Patients ≥12 Years of Age with Inhibitors

Endpoint	QFITLIA AT-DR (N=38)	On-Demand BPA (N=19)
ABR = annualized bleed rate; AT-DR = AT-Dosing Regimen; BPA = bypassing agents; CI = confidence interval.
All Treated Bleeds
ABR (95% CI) Based on negative binomial regression model.	5.1 (2.8, 9.5)	19.1 (11.8, 31.0)
% reduction p-value	73% p=0.0006
Treated Spontaneous Bleeds
ABR (95% CI)	3.1 (1.8, 5.4)	17.1 (9.9, 29.6)
% reduction p-value	82% <0.0001
Treated Joint Bleeds
ABR (95% CI)	4.0 (2.5, 6.2)	14.4 (9.0, 23.1)
% reduction p-value	73% p=0.0001

Table 6: Annualized Bleed Rate for Treated Bleeds with QFITLIA Prophylaxis versus On-Demand CFC in Patients ≥12 Years of Age without Inhibitors

Endpoint	QFITLIA AT-DR (N=80)	On-Demand CFC (N=40)
ABR = annualized bleed rate; AT-DR = AT-Dosing Regimen; CFC = clotting factor concentrate; CI = confidence interval.
All Treated Bleeds
ABR (95% CI) Based on negative binomial regression model.	9.0 (5.6, 14.5)	31.4 (20.5, 48.2)
% reduction p-value	71% p<0.0001
Treated Spontaneous Bleeds
ABR (95% CI)	5.4 (3.7, 8.0)	21.0 (14.0, 31.6)
% reduction p-value	74% p<0.0001
Treated Joint Bleeds
ABR (95% CI)	6.2 (4.2, 9.2)	21.6 (14.6, 31.9)
% reduction p-value	71% p<0.0001

50 mg Prefilled Pen

• Store refrigerated at 2°C to 8°C (36°F to 46°F) in the original carton to protect from light.
• QFITLIA may be stored at room temperature between 15°C to 30°C (59°F to 86°F) for a single period of up to 3 months within the expiration date printed on the label. Discard no later than 3 months after removal from the refrigerator or at the expiration date, whichever comes first. After storage at room temperature, do not return the product to the refrigerator.

20 mg Vial

• Store QFITLIA either in the refrigerator at 2°C to 8°C (36°F to 46°F) or at room temperature between 15°C to 30°C (59°F to 86°F), in the original carton to protect from light. After storage at room temperature, do not return the product to the refrigerator.

Do not shake QFITLIA at any time. Do not heat QFITLIA. Do not freeze. Do not put into direct sunlight.

Use of BPAs or CFCs

Advise the patient and/or caregiver to discontinue prophylactic use of BPA or CFC no later than 7 days after starting QFITLIA to reduce the risk of thrombotic events. Discuss the appropriate dosing and frequency of BPA or CFC for breakthrough bleed management with the patient and/or caregiver prior to starting QFITLIA prophylaxis [see Dosage and Administration (2.3)].

Thrombotic Events

Advise the patient and/or caregiver of the risk of thrombotic events while receiving QFITLIA. Inform the patient and/or caregiver of the need for periodic measurements of AT activity that may result in changes to the QFITLIA dose and/or frequency of administration to reduce the risk for thrombosis. Educate patients on the signs and symptoms of thrombotic events and to seek immediate medical attention if new symptoms of thrombotic events occur [see Warnings and Precautions (5.1)].

Acute and Recurrent Gallbladder Disease

Inform the patient and/or caregiver of the risk of acute and recurrent gallbladder disease while receiving QFITLIA. Educate patients on the signs and symptoms of gallbladder disease and to seek medical attention if new symptoms of gallbladder disease occur [see Warnings and Precautions (5.2)].

Hepatotoxicity

Inform the patient and/or caregiver of the risk of hepatotoxicity and that blood tests to monitor for this risk will be obtained before starting QFITLIA and periodically during treatment. Inform patients to seek medical attention if symptoms of hepatotoxicity occur [see Warnings and Precautions (5.3)].

Administration Instructions

Provide training to the patient and/or caregiver on proper subcutaneous injection technique, including aseptic technique, and the preparation and administration of QFITLIA prior to use [see Dosage and Administration (2.4)].

Manufactured by:
Genzyme Corporation
Cambridge, MA 02141
A SANOFI COMPANY
© 2025 GENZYME CORPORATION. All rights reserved.

For patent information: https://www.sanofi.us/en/products-and-resources/patents

QFITLIA is a trademark of GENZYME CORPORATION

QFITLIA is indicated for routine prophylaxis to prevent or reduce the frequency of bleeding episodes in adult and pediatric patients aged 12 years and older with hemophilia A or B with or without factor VIII or IX inhibitors.

For subcutaneous use only.

Use of QFITLIA is recommended under the supervision of a healthcare professional experienced in the treatment of hemophilia or bleeding disorders.

Monitor AT activity using an FDA-cleared test. Information on FDA-cleared tests for AT activity is available at http://www.fda.gov/CompanionDiagnostics.

Measure AT activity prior to initiation of QFITLIA. Do not initiate QFITLIA dosing if AT activity is <60%.

After QFITLIA is initiated, patients may continue their prior clotting factor concentrates (CFC) or bypassing agent (BPA) prophylaxis for the first 7 days of treatment. Discontinue CFC or BPA prophylaxis no later than 7 days after the initial dose of QFITLIA.

The starting dose of QFITLIA is 50 mg once subcutaneously every two months. Adjust the dose and/or dosing interval, if needed, to maintain AT activity between 15–35% [see Boxed Warning, Dosage and Administration (2.2) and Warnings and Precautions (5.1)].

Measure AT activity using an FDA-cleared test at Weeks 4 (Month 1), 12 (Month 3), 20 (Month 5) and 24 (Month 6) following the starting dose and after any dose modification.

• If any AT activity is <15%, a dose reduction is required. The lower dose should be initiated 3 months after the prior dose. AT measurements should be restarted after a dose reduction.
• If AT activity is >35% after 6 months, or if the patient has not achieved satisfactory bleed control, dose escalation should be considered. AT measurements should be restarted after a dose escalation.

Refer to Table 1 below for modified dosage based on AT activity levels.

Table 1: Dose Modification Based on Antithrombin Activity Levels

Last Dosage Administered	Antithrombin Activity Level	Dose Modification
50 mg every 2 months	Less than 15%	20 mg every 2 months
	15% to 35%	Continue current dosage
	Greater than 35% after 6 months	50 mg every month
20 mg every 2 months	Less than 15%	10 mg every 2 months
	15% to 35%	Continue current dosage
	Greater than 35% after 6 months	20 mg every month
10 mg every 2 months	Less than 15%	Discontinue QFITLIA
	15% to 35%	Continue current dosage
	Greater than 35% after 6 months	10 mg every month

Once the patient's target dose is identified based on AT activity 15–35%, measure AT activity annually. Additional AT measurements can be considered if bleeding control is not adequate.

After cessation of QFITLIA dosing, routine AT monitoring is not needed unless the patient is bleeding and treatment with CFC/BPA is required. Based on data from the clinical studies, a majority of patients have AT activity >60% by 6 months after the last QFITLIA dose, after which standard doses of CFC/BPA may be used.

QFITLIA is intended for use under the guidance of a healthcare provider. Provide proper training to patients and/or caregivers on the preparation and administration of QFITLIA prior to use, according to the Instructions for Use (IFU). A patient may self-inject QFITLIA or the patient's caregiver may administer QFITLIA. In pediatric patients 12 to 17 years of age, it is recommended that QFITLIA be administered by or under the supervision of an adult.

QFITLIA for subcutaneous administration is a clear, colorless to pale yellow solution. Do not use if the solution is discolored or cloudy, or if it contains visible flakes or particles. Do not use QFITLIA if it has been dropped or damaged.

If QFITLIA is stored at room temperature, it is ready for use. If QFITLIA is stored in the refrigerator, remove from the refrigerator and allow QFITLIA to reach room temperature, for at least 30 minutes.

Administer QFITLIA by subcutaneous injection in the thigh or abdomen region, except for the 2 inches (5 cm) around the navel. A caregiver can also inject QFITLIA in the outer area of the patient's upper arm. QFITLIA should not be injected into skin that is tender, damaged, bruised, or scarred. Do not inject into a vein.

To inject 10 mg or 20 mg of QFITLIA from the single-dose vial, it is recommended to use a sterile 1 mL Luer Lock syringe (polypropylene or polycarbonate), and a sterile 27 gauge ½ inch (13 mm) Luer Lock needle to withdraw and inject QFITLIA solution subcutaneously (see the Instructions for Use).

Discard unused product remaining in the prefilled pen or vial.

QFITLIA is a clear, colorless to pale yellow solution in a single-dose:

• Injection: 50 mg/0.5 mL prefilled pen
• Injection: 20 mg/0.2 mL vial

None.

Serious thrombotic events have been reported in QFITLIA-treated patients. Thrombotic events were reported in 2.6% of patients receiving the 80 mg once monthly dose (2.3 events per 100 person-years), including a fatal event of cerebral venous sinus thrombosis. The 80 mg once monthly dose is not approved or recommended for use. Thrombotic events were reported in 1.4% of patients receiving QFITLIA prophylaxis using the antithrombin-based dose regimen (AT-DR) that targeted AT activity 15-35% (0.8 events per 100 person-years). Participants with established thrombophilia or a history of thrombosis were generally excluded from studies with QFITLIA.

The risk of thrombosis is greater in patients with persistent AT activity <15%, with comorbidities that predispose to thrombosis, when bleed management guidelines are not followed in the post-operative setting, when there is an indwelling venous catheter, and with use of the 80 mg once monthly (non-AT-based) dose. Treatment of breakthrough bleeding episodes with CFC or BPA at a dose greater or more frequent than recommended may also increase thrombotic risk [see Dosage and Administration (2.3)]. The decision to utilize higher dosing regimens of CFC or BPA in the setting of inadequate hemostasis requires an assessment of the benefits and risks and close clinical monitoring.

Monitor AT activity using an FDA-cleared test and target AT activity 15–35% to reduce the risk of thrombosis [see Dosage and Administration (2.1, 2.2) and Warnings and Precautions (5.1)]. Monitor patients for signs and symptoms of thrombotic events. Interrupt QFITLIA prophylaxis in patients with a thrombotic event and manage as clinically indicated.

Inform patients treated with QFITLIA to monitor for and report signs and symptoms of thrombotic events. Consider the benefits and risks of resuming QFITLIA prophylaxis following resolution of the thrombotic event.

Treatment with QFITLIA is associated with an increased occurrence of acute and recurrent gallbladder disease including cholelithiasis and cholecystitis. QFITLIA at a fixed dose (including 80 mg once monthly) is not approved or recommended for use. In the 270 patients in the QFITLIA clinical studies who received the fixed dose (non-AT-based dose) once monthly regimen, 17% experienced gallbladder events and 4% (11 patients) underwent cholecystectomy.

In 286 patients who received the AT-DR, 3.8% experienced gallbladder events and 0.3% (1 patient) underwent cholecystectomy.

All but one of the patients who underwent cholecystectomy resumed QFITLIA after surgery. One patient who started on fixed dosing experienced cholangitis and pancreatitis caused by gallstone disease more than a year after cholecystectomy while receiving AT-DR.

Patients diagnosed with acute or recurrent gallbladder disease most commonly presented with epigastric pain, generalized abdominal pain, indigestion, nausea and/or vomiting. If gallbladder disease is suspected, appropriate imaging and clinical follow-up are indicated.

Consider alternative treatment for hemophilia in patients with a history of symptomatic gallbladder disease. Consider interruption or discontinuation of QFITLIA if gallbladder disease occurs.

In the two randomized studies testing QFITLIA 80 mg once monthly, serum alanine transaminase (ALT) and aspartate transaminase (AST) elevations above 3 times the upper limit of normal (ULN) occurred in 32% of patients with hemophilia with inhibitors and 18% of patients with hemophilia without inhibitors compared to no events of AST or ALT elevation greater than 3× ULN in the control groups. There was one case of moderate hepatic injury (ALT elevation >300 U/L and total serum bilirubin >3 mg/dL) attributable to QFITLIA use. This patient had elevation of liver tests after a single 80 mg dose that continued to rise with repeated dosing of QFITLIA 80 mg once monthly. This patient's liver tests recovered with drug discontinuation. QFITLIA 80 mg once monthly is not approved or recommended for use.

On the AT-DR, 3.4% of patients treated with QFITLIA had at least one ALT value greater than 3× ULN with a median onset of 89 days after initial dosing (range 15 to 768 days).

Avoid use of QFITLIA in patients with hepatic impairment (Child-Pugh Class A, B and C).

Obtain baseline liver tests including AST, ALT, and total bilirubin prior to initiating QFITLIA, monthly for at least the first 6 months of QFITLIA use, and monthly for at least 6 months after a dose increase, and periodically thereafter as clinically indicated.

If new or worsening liver test abnormalities occur, perform appropriate diagnostic evaluations, initiate medical management as appropriate and monitor laboratory parameters until they return to baseline. If ALT or AST elevations greater than 5× ULN occur, interrupt QFITLIA treatment. Consider the benefits and risks of resuming QFITLIA prophylaxis following resolution of transaminase elevations. If you decide to restart QFITLIA, wait until liver tests have returned to baseline. If QFITLIA is restarted and ALT or AST elevations greater than 5× ULN reoccur or the patient experiences jaundice (total bilirubin ≥2.5 mg/dL) thought to be from hepatotoxicity with other causes of liver test elevation ruled out, permanently discontinue QFITLIA.

The following clinically significant adverse reactions are described elsewhere in the labeling:

• Thrombotic Events [see Boxed Warning and Warnings and Precautions (5.1)]
• Acute and Recurrent Gallbladder Disease [see Boxed Warning and Warnings and Precautions (5.2)]
• Hepatotoxicity [see Warnings and Precautions (5.3)]

Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.

The pooled safety population described in the WARNINGS AND PRECAUTIONS reflect exposure to QFITLIA as fixed doses and AT-DR (N=335).

The safety of the QFITLIA AT-DR was assessed in 286 adult and pediatric male patients with hemophilia A or B with or without inhibitors [see Clinical Studies (14)].

Among patients who received the AT-DR, 93% were exposed for 6 months or longer and 83% were exposed for 12 months or longer. The median duration of exposure across the studies was 674 days (with a maximum of 896 days).

Serious adverse reactions occurred in 4/286 (1.4%) patients who received the AT-DR, two of whom had serious adverse reactions of cholecystitis.

Permanent discontinuation of QFITLIA due to an adverse reaction occurred in 4/286 (1.4%) patients receiving the AT-DR and included liver injury, post-operative deep vein thrombosis, cerebral infarction and pruritus.

Dosage interruptions of QFITLIA due to an adverse reaction occurred in 2/286 (0.7%) patients receiving the AT-DR and included increased serum transaminases.

The most common adverse reactions (≥10%) reported in patients treated with the AT-DR were viral infection, nasopharyngitis, and bacterial infection.

QFITLIA prophylaxis leads to increased thrombin generation with additive increase in peak thrombin when used concomitantly with CFC or BPA [see Boxed Warning, Dosage and Administration (2.3) and Warnings and Precautions (5.1)].

The safety and effectiveness of QFITLIA for the treatment of hemophilia A or B with or without factor VIII or IX inhibitors have been established in pediatric patients aged 12 years and older. Use of QFITLIA in pediatric patients with hemophilia A and B is supported by evidence from adequate and well-controlled studies in adult and pediatric patients [see Adverse Reactions (6.1) and Clinical Studies (14)]. A total of 60 pediatric patients ages 12 to 17 were treated with QFITLIA in the clinical studies.

The safety and effectiveness of QFITLIA have not been established in pediatric patients below 12 years of age.

There were 3 patients with hemophilia 65 years of age and older in the clinical studies on QFITLIA. Clinical studies of QFITLIA did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects.

Serum transaminase elevations have been observed in the clinical studies [see Warnings and Precautions (5.3)]. Avoid use of QFITLIA in patients with established hepatic impairment (Child-Pugh Class A, B and C).

QFITLIA injection contains fitusiran, an antithrombin-directed double-stranded small interfering ribonucleic acid (siRNA), which is covalently linked to a ligand containing a triantennary N-acetylgalactosamine (GalNAc) moiety. The molecular formula of fitusiran sodium is C₅₂₀H₆₃₆F₂₁N₁₇₅Na₄₃O₃₀₉P₄₃S₆ and the molecular weight is 17,193 Da. Fitusiran drug substance is a white to pale yellow powder and freely soluble in water and phosphate buffered saline. The pH of a 1% aqueous solution of fitusiran drug substance in 50 mM KCl is 5.4 (4.4–7.3). It has the following structural formula:

Chemical Structure (6dd2f8ac 6f90 4cbf B197 97d74964135c 01)

QFITLIA is supplied as a sterile, preservative-free, clear, colorless to pale yellow solution for subcutaneous administration.

Each 50 mg single-dose prefilled pen delivers 50 mg fitusiran (equivalent to 53.0 mg fitusiran sodium) in 0.5 mL, and also contains dibasic sodium phosphate (0.585 mg), monobasic sodium phosphate (0.044 mg), sodium chloride (2.455 mg), and Water for Injection, USP. Phosphoric acid (concentrated) and sodium hydroxide may be added to adjust to pH 7.0.

Each 20 mg single-dose vial delivers 20 mg fitusiran (equivalent to 21.2 mg fitusiran sodium) in 0.2 mL, and also contains dibasic sodium phosphate (0.234 mg), monobasic sodium phosphate (0.018 mg), sodium chloride (0.982 mg), and Water for Injection, USP. Phosphoric acid (concentrated) and sodium hydroxide may be added to adjust to pH 7.0.

QFITLIA is a double-stranded siRNA that causes degradation of AT messenger RNA (mRNA) through RNA interference, reducing plasma AT levels.

In clinical studies with QFITLIA in hemophilia patients, the primary pharmacodynamic (PD) measure was plasma AT activity. Lower AT activity levels were associated with lower annualized bleeding rates (ABR); however, persistent AT activity <15% is a risk factor for thrombotic events.

In Study LTE15174, the mean (SD) AT activity on the AT-DR was 24% (4.64).

Simulations to estimate time for AT activity to reach steady state found that regardless of the dose regimen, more than 99% of participants reached steady state AT levels (defined as <10% variability among consecutive measures) within 23 weeks following initiation of QFITLIA dosing or following dose escalation or de-escalation. The duration of persistent AT activity <60% (non-negligible impact of QFITLIA on coagulation) following QFITLIA treatment discontinuation was estimated to be approximately 6 months, after which standard doses of CFC/BPA may be administered. In patients with AT activity <15%, the time required prior to initiation of a lower dose was estimated to be 12 weeks to maximize the AT activity recovery to the target range of 15% to 35%. Extent of AT reduction with QFITLIA did not differ between patients with hemophilia A or B, with or without inhibitors.

The pharmacokinetic (PK) properties of fitusiran were evaluated following administration of QFITLIA in patients with hemophilia A or B, with or without inhibitors as summarized in Table 4. QFITLIA PD is driven by liver PK rather than plasma PK. The QFITLIA dosing strategy is based on maintaining plasma AT activity levels between 15–35% with 10, 20 or 50 mg dosing every month or every two months.

The observed incidence of anti-drug antibodies (ADA) is highly dependent on the sensitivity and specificity of the assay. Differences in assay methods preclude meaningful comparisons of the incidence of ADA in the studies described below with the incidence of ADA in other studies, including those of QFITLIA or of other fitusiran products.

During QFITLIA treatment (up to 250 weeks) in four studies, 10 out of 290 adults with hemophilia (3.4%) developed ADAs. All patients had low ADA titers, and the majority of patients had transient ADAs. There was no identified clinically significant effect of ADAs on PK, PD, safety, or effectiveness of QFITLIA.

In a 2-year carcinogenicity study in Sprague Dawley rats, fitusiran was not carcinogenic up to the highest dose tested following subcutaneous administration at doses of 0.03, 0.1 or 0.3 mg/kg/week in males and 0.1, 0.3, or 1 mg/kg/week in females. All doses in males and females were below the maximum recommended human dose (MRHD) of 50 mg per month based on body surface area (BSA) comparisons due to the sensitivity of wild type animals to the pharmacological effects of fitusiran. Fitusiran was not carcinogenic in Tg-rasH2 mice following subcutaneous administration at doses of 0.05, 0.15, or 0.5 mg/kg/week in males and 0.025, 0.08, or 0.25 mg/kg/week in females for 26 weeks.

Fitusiran was not mutagenic or clastogenic in a battery of genetic toxicity studies (i.e., in vitro bacterial reverse mutation assay, in vitro chromosomal aberration assay in human peripheral blood lymphocytes; in vivo bone marrow micronucleus test in rats).

In a chronic repeat dose toxicology study in Sprague Dawley rats, fitusiran-treated males received subcutaneous doses of 0.25, 0.5, or 1 mg/kg/week for 16 weeks then were cohabitated with fitusiran-naïve females. No adverse effects on male fertility endpoints were observed. All doses used in males were below the MRHD based on BSA comparisons due to the sensitivity of wild type animals to the pharmacological effects of fitusiran.

The efficacy and safety of QFITLIA in adult and pediatric patients aged 12 years and older with hemophilia A or B with or without inhibitors were established in two clinical studies:

• Hemophilia A or B with Inhibitory Antibodies: ATLAS-INH (NCT03417102)
• Hemophilia A or B without Inhibitory Antibodies: ATLAS-A/B (NCT03417245)

Patients in the above parent studies rolled over into the long-term extension study ATLAS-OLE (NCT03754790).

The clinical studies ATLAS-INH and ATLAS-A/B tested an 80 mg monthly fixed dose of QFITLIA. Because of thrombotic events with this dose, the QFITLIA AT-DR targeting AT activity of 15–35% was implemented in ATLAS-OLE. The AT-DR was initiated when studies ATLAS-INH and ATLAS-A/B were nearly completed, therefore, the efficacy of QFITLIA AT-DR treatment was assessed by comparing the QFITLIA AT-DR treatment data from the long-term extension study ATLAS-OLE to the control data from studies ATLAS-INH and ATLAS-A/B. The efficacy analyses were conducted according to the intent to treat (ITT) principle preserving the randomization in the parent studies.

QFITLIA (fitusiran) is a clear, colorless to pale yellow solution supplied in a single-dose prefilled pen or a single-dose vial. Each prefilled pen is designed to deliver 50 mg of QFITLIA in 0.5 mL (NDC 58468-0348-1). Each vial is designed to deliver 20 mg of QFITLIA in 0.2 mL (NDC 58468-0347-1).

QFITLIA is available in cartons containing 1 prefilled pen or 1 vial.

• Advise the patient to read the FDA-approved patient labeling (Medication Guide and Instructions for Use).

QFITLIA™ (kew fit lee ah)
(fitusiran)
injection, for subcutaneous use
Single-Dose Prefilled Pen (50 mg/0.5 mL)

This Instructions for Use contains information on how to inject QFITLIA.

Read this Instructions for Use before using the QFITLIA Prefilled Pen. Do not inject yourself or someone else until you have been shown how to inject QFITLIA Prefilled Pen. Your healthcare provider can show you or your caregiver how to prepare and inject a dose of QFITLIA before you try to do it yourself for the first time. Keep this Instructions for Use. Call your healthcare provider if you have any questions.

QFITLIA Prefilled Pen is only for use in adults and children 12 years of age and older. It is recommended that QFITLIA Prefilled Pen be given by adults or under adult supervision to children 12 to 17 years of age.

This QFITLIA Prefilled Pen is a single-dose device. It contains 50 mg of QFITLIA for injection under the skin (subcutaneous injection).

The parts of the QFITLIA Prefilled Pen are shown below:

Image (6dd2f8ac 6f90 4cbf B197 97d74964135c 02)

Important information to know before injecting QFITLIA

• Read all of the instructions carefully before using the QFITLIA Prefilled Pen.
• Ask your healthcare provider how often you will need to inject the medicine.
• Throw away (dispose of) the used QFITLIA Prefilled Pen right away after use.
• Do not re-use a QFITLIA Prefilled Pen.
• QFITLIA Prefilled Pen is for subcutaneous use only. Do not inject QFITLIA Prefilled Pen into a vein.

Storing QFITLIA Prefilled Pen

• Store QFITLIA Prefilled Pen in the refrigerator between 36°F to 46°F (2°C to 8°C) in the original carton to protect from light.
• QFITLIA Prefilled Pen may be stored at room temperature between 59°F to 86°F (15°C to 30°C) for a single period of up to 3 months within the expiration date printed on the label.
• Do not return QFITLIA Prefilled Pen to the refrigerator after storing at room temperature.
• Do not shake the QFITLIA Prefilled Pen at any time.
• Do not heat the QFITLIA Prefilled Pen.
• Do not freeze the QFITLIA Prefilled Pen.
• Do not put the QFITLIA Prefilled Pen into direct sunlight.
• Keep QFITLIA Prefilled Pen and all medicines out of the reach of children.

A. Get ready to inject

A1) Gather supplies

Find a clean, flat work surface. Make sure you have the following supplies:



Image (6dd2f8ac 6f90 4cbf B197 97d74964135c 03)

A2) Check the QFITLIA Prefilled Pen

• Note: The plunger stopper in the middle of the Window is normal.
  
  

  Image (6dd2f8ac 6f90 4cbf B197 97d74964135c 04)

• Do not use the QFITLIA Prefilled Pen if it has been dropped or damaged.
• Do not use the QFITLIA Prefilled Pen if the Blue Cap is missing or not securely attached.
• Do not use the QFITLIA Prefilled Pen if the Window is yellow before use. A yellow Window means the QFITLIA Prefilled Pen has been used.
  
  

  Image (6dd2f8ac 6f90 4cbf B197 97d74964135c 05)

A3) Look at the label



Image (6dd2f8ac 6f90 4cbf B197 97d74964135c 06)

• Check the label to be sure that you have the correct prescribed medicine and dose.


Image (6dd2f8ac 6f90 4cbf B197 97d74964135c 07)

• Check the expiration date.
• Do not use the QFITLIA Prefilled Pen if the expiration date has passed.

A4) Check the medicine



Image (6dd2f8ac 6f90 4cbf B197 97d74964135c 08)

• Look at the medicine through the Window, it should be clear and colorless to pale yellow.
• Note: You may see air bubbles, this is normal.
• Do not use the QFITLIA Prefilled Pen if the liquid is discolored or cloudy, or if it contains visible flakes or particles.

A5) If QFITLIA Prefilled Pen was stored in the refrigerator, warm up for 30 minutes.



Image (6dd2f8ac 6f90 4cbf B197 97d74964135c 09)

• Lay the QFITLIA Prefilled Pen on a clean, flat surface and let it warm up at room temperature between 59°F to 86°F (15°C to 30°C) for at least 30 minutes.
• Do not heat the QFITLIA Prefilled Pen or put into direct sunlight.

B. Choose and prepare your injection site

B1) Wash your hands well with soap and water



Image (6dd2f8ac 6f90 4cbf B197 97d74964135c 10)

B2) Choose an injection site

• Thigh
• Stomach except for the 2 inches (5 cm) around your belly button (navel).
• A caregiver can also inject in the outer area of your upper arm.
• Do not inject into skin that is tender, damaged, has bruises or scars, or into areas with visible veins.
• For subcutaneous use only. Do not inject into a vein.
• Do not inject through clothes.


Image (6dd2f8ac 6f90 4cbf B197 97d74964135c 11)

B3) Prepare the injection site



Image (6dd2f8ac 6f90 4cbf B197 97d74964135c 12)

• Clean the injection site with an alcohol wipe.
• Let the skin dry before injecting.
• Do not touch the injection site again or blow on it before the injection.

C. Give the injection

C1) Remove Blue Cap



Image (6dd2f8ac 6f90 4cbf B197 97d74964135c 13)

• Remove the Blue Cap by pulling it straight off as shown. Do not twist the Blue Cap off.
• Do not remove the Blue Cap until you are ready to inject.
• Do not touch the Orange Needle Cover with your fingers. The Needle is inside.
• Do not put the Blue Cap back on the QFITLIA Prefilled Pen after you have removed it.
• Note: You may see a droplet on the needle tip. This is normal.

C2) Place QFITLIA Prefilled Pen on injection site



Image (6dd2f8ac 6f90 4cbf B197 97d74964135c 14)

• Hold the QFITLIA Prefilled Pen as shown so you can see the Window.
• Place the Orange Needle Cover on the skin at a 90-degree angle.

C3) Press down firmly → Watch Window turn fully yellow



Image (6dd2f8ac 6f90 4cbf B197 97d74964135c 15)

Press down and hold the QFITLIA Prefilled Pen firmly against the skin until you cannot see the Orange Needle Cover.

• There will be a "click" when the injection starts, and
• The Window will start to turn yellow.


Image (6dd2f8ac 6f90 4cbf B197 97d74964135c 16)

Keep pressing the QFITLIA Prefilled Pen against the skin and watch the Window.



Image (6dd2f8ac 6f90 4cbf B197 97d74964135c 17)

• The Window will turn completely yellow, and
• You may hear a 2nd "click." The injection is complete.

C4) Remove



Image (6dd2f8ac 6f90 4cbf B197 97d74964135c 18)

• After you have completed your injection pull straight up to remove QFITLIA Prefilled Pen from the skin. The Orange Needle Cover will cover the needle.
• If you see any blood at the site, lightly dab a cotton ball or gauze pad.
• Do not rub the skin after the injection.
• If the Window does not turn completely yellow, or if it looks like you may not have received a full dose, call your healthcare provider right away.
• Do not give a second dose without speaking to your healthcare provider.

D. Throw away (dispose of) used QFITLIA Prefilled Pen



Image (6dd2f8ac 6f90 4cbf B197 97d74964135c 19)

• Do not put the Blue Cap back on.

Keep your sharps disposal container out of the reach of children.

How to dispose of (throw away) QFITLIA Prefilled Pen

• Put your used QFITLIA Prefilled Pen and Blue Cap in an FDA-cleared sharps disposal container right away after use.
• Do not dispose of (throw away) QFITLIA Prefilled Pen and Blue Cap in your household trash.
• If you do not have an FDA-cleared sharps disposal container, you may use a household container that is:
  • made of a heavy-duty plastic,
  • can be closed with a tight-fitting, puncture-resistant lid, without sharps being able to come out,
  • upright and stable during use,
  • leak-resistant, and
  • properly labeled to warn of hazardous waste inside the container.
  • When your sharps disposal container is almost full, you will need to follow your community guidelines for the right way to dispose of your sharps disposal container. There may be state or local laws about how you should throw away used QFITLIA Prefilled Pens.
  • For more information about safe sharps disposal, and for specific information about sharps disposal in the state that you live in, go to the FDA's website at: http://www.fda.gov/safesharpsdisposal
  • Do not dispose of your used sharps disposal container in your household trash unless your community guidelines permit this.
  • Do not recycle your used sharps disposal container.

  Manufactured by:
  Genzyme Corporation
  Cambridge, MA 02141
  A SANOFI COMPANY

  QFITLIA is a trademark of GENZYME CORPORATION
  © 2025 GENZYME CORPORATION. All rights reserved.

  For patent information: https://www.sanofi.us/en/products-and-resources/patents

  For more information go to www.QFITLIA.com or call 1-800-745-4447.

  This Instructions for Use has been approved by the US Food and Drug Administration.
  Issued: March 2025

  QFITLIA™ (kew fit lee ah)
  (fitusiran)
  injection, for subcutaneous use
  Single-Dose Vial (20 mg/0.2 mL)

  This Instructions for Use contains information on how to inject QFITLIA from a vial.

  Read this Instructions for Use before using QFITLIA. Do not inject yourself or someone else until you have been shown how to inject QFITLIA from a vial. Your healthcare provider can show you or your caregiver how to prepare and inject a dose of QFITLIA from a vial before you do it yourself for the first time. Keep this Instructions for Use. Call your healthcare provider if you have any questions.

  QFITLIA is only for use in adults and children 12 years of age and older. In children 12 to 17 years of age it is recommended that QFITLIA be given by or under the supervision of an adult.

  This QFITLIA vial is for single-use only. It contains 20 mg of QFITLIA for injection under the skin (subcutaneous injection).

  Important information to know before injecting QFITLIA

  • Read all of the instructions carefully before using QFITLIA.
  • Ask your healthcare provider how often you will need to inject the medicine.
  • Check your prescription label to make sure you draw up the correct medicine dose prescribed by your healthcare provider.
  • Throw away (dispose of) the used vial, syringe and needle right away after use.
  • Only use the vial one time. After you inject your dose, throw away (dispose of) any unused QFITLIA left in the vial. Do not save any unused QFITLIA in the vial for later use.
  • QFITLIA is for subcutaneous use only. Do not inject QFITLIA into a vein.

  Storing QFITLIA vial

  • Store QFITLIA vial either in the refrigerator between 36°F to 46°F (2°C to 8°C) or at room temperature between 59°F to 86°F (15°C to 30°C) in the original carton to protect from light.
  • Do not return QFITLIA vial to the refrigerator after storing at room temperature.
  • Do not shake the QFITLIA vial at any time.
  • Do not heat the QFITLIA vial.
  • Do not freeze the QFITLIA vial.
  • Do not put the QFITLIA vial into direct sunlight.
  • Keep QFITLIA vial and all medicines out of the reach of children.

  A. Get ready to inject

  A1) Gather the supplies.

  Find a clean, flat work surface. Make sure you have the following supplies:

  

  Image (6dd2f8ac 6f90 4cbf B197 97d74964135c 20)

  A2) Check the vial.

  • Do not use the QFITLIA vial if it has been dropped or damaged.
  • Check the label on the vial to be sure that you have the correct prescribed medicine and dose.
  • Check expiration date (EXP:).
  • Do not use QFITLIA if the expiration date on the vial has passed.
  

  Image (6dd2f8ac 6f90 4cbf B197 97d74964135c 21)

  A3) Check the medicine.

  • Look at the medicine in the vial to make sure it is clear and colorless to pale yellow.
  • Do not use QFITLIA if the liquid in the vial is discolored or cloudy, or if it contains visible flakes or particles.

  A4) If the QFITLIA vial was stored in the refrigerator, warm up for 30 minutes.

  • Set the QFITLIA vial on a clean, flat surface and let it warm up at room temperature between 59°F to 86°F (15°C to 30°C) for at least 30 minutes.
  • Do not heat the QFITLIA vial or put in direct sunlight.

  A5) Wash your hands well with soap and water.

  A6) Remove the protective cap from the QFITLIA vial.
  Do not remove the stopper.

  

  Image (6dd2f8ac 6f90 4cbf B197 97d74964135c 22)

  A7) Wipe the rubber stopper of the vial with an alcohol wipe and allow it to dry.

  

  Image (6dd2f8ac 6f90 4cbf B197 97d74964135c 23)

  B. Choose and prepare the injection site

  B1) Choose the injection site.

  • Thigh
  • Stomach except for the 2 inches (5 cm) around your belly button (navel).
  • A caregiver can also inject in the outer area of your upper arm.
  • Do not inject into skin that is tender, damaged, has bruises or scars, or into areas with visible veins.
  • Do not inject into a vein. For subcutaneous use only.
  • Do not inject through clothes.
  

  Image (6dd2f8ac 6f90 4cbf B197 97d74964135c 24)

  B2) Prepare the injection site.

  • Clean the injection site with an alcohol wipe.
  • Let the skin dry before injecting.
  • Do not touch the injection site again or blow on it before the injection.

  C. Prepare the injection
  Contact your healthcare provider if you have any questions about preparing your dose.

  C1) Attach the needle to the syringe and remove the needle cap.

  • Attach the needle to the syringe.
  • Hold the syringe body and pull the needle cap straight off the syringe.
  • Do not touch the needle.
  • Do not recap the needle.

  C2) Withdraw the solution.

  Withdraw slightly more than your prescribed dose into the syringe.

  • Push the needle through the center of the rubber vial stopper.
  • Leave the needle in the vial and turn both the syringe and vial upside down (vial on top).
  • Hold the syringe and vial firmly in one hand. Make sure the tip of the needle is in the QFITLIA solution.
  • With your other hand, pull back on the plunger rod to withdraw slightly more than your prescribed dose into the syringe.
    • Withdraw slightly more than 0.2 mL for a 20 mg dose.
    • Withdraw slightly more than 0.1 mL for a 10 mg dose.
    

    Image (6dd2f8ac 6f90 4cbf B197 97d74964135c 25)

    C3) Check for air bubbles.

    • Keep the needle in the vial and make sure both syringe and vial are upside down (vial on top).
    • If air bubbles are in the syringe, hold the syringe straight up and tap the side of the syringe until the bubbles float to the top.
    • Push the plunger rod up to push the bubbles out of the syringe.
      

      Image (6dd2f8ac 6f90 4cbf B197 97d74964135c 26)

    C4) Adjust plunger to your prescribed dose.

    • Push the plunger rod to push solution back into the vial until you have the prescribed dose in the syringe.
      • Push plunger rod to 0.2 mL for a 20 mg dose.
      • Push plunger rod to 0.1 mL for a 10 mg dose.
      • If the medicine in the syringe is less than your prescribed dose, repeat steps C2, C3 and C4 until you have your correct dose.
      • Remove the needle from the vial. Do not let the needle touch anything.

      Image (6dd2f8ac 6f90 4cbf B197 97d74964135c 27)

      Image (6dd2f8ac 6f90 4cbf B197 97d74964135c 28)

      D. Inject QFITLIA

      D1) Pinch a fold of skin and insert the needle.

      Gently pinch a fold of skin at the cleaned injection site. Insert the needle into the skin fold at a 45° to 90° angle.

      

      Image (6dd2f8ac 6f90 4cbf B197 97d74964135c 29)

      D2) Inject QFITLIA.

      Relax the skin pinch. Slowly push the plunger rod all the way to the bottom of the syringe body and inject all of the QFITLIA solution.

      

      Image (6dd2f8ac 6f90 4cbf B197 97d74964135c 30)

      D3) Gently pull out the needle and syringe from the injection site.

      • Do not recap the used needle to avoid a needle-stick injury.
      • Do not rub the skin after the injection.
      • If you see any blood at the site, lightly dab it with a cotton ball or gauze pad. If your injection site becomes red or sore, call your healthcare provider right away.

      E. Throw away (dispose of) used vial, needle and syringe

      E1) Throw away (dispose of) your used vial, needle and syringe in an FDA-cleared sharps disposal container right away after use.

      Do not re-use the vial, needle, or syringe.

      

      Image (6dd2f8ac 6f90 4cbf B197 97d74964135c 31)

      Keep your sharps disposal container out of the reach of children.

      If you do not have an FDA-cleared sharps disposal container, you may use a household container that is:

      • made of a heavy-duty plastic,
      • can be closed with a tightfitting, puncture-resistant lid, without sharps being able to come out,
      • upright and stable during use,
      • leak-resistant, and
      • properly labeled to warn of hazardous waste inside the container.

      When your sharps disposal container is almost full, you will need to follow your community guidelines for the right way to dispose of your sharps disposal container. There may be state or local laws about how you should throw away used QFITLIA needles and syringes.

      For more information about safe sharps disposal, and for specific information about sharps disposal in the state that you live in, go to the FDA's website at: http://www.fda.gov/safesharpsdisposal

      • Do not dispose of your used sharps disposal container in your household trash unless your community guidelines permit this.
      • Do not recycle your used sharps disposal container.

      Manufactured by:
      Genzyme Corporation
      Cambridge, MA 02141
      A SANOFI COMPANY

      QFITLIA is a trademark of GENZYME CORPORATION
      © 2025 GENZYME CORPORATION. All rights reserved.

      For patent information: https://www.sanofi.us/en/products-and-resources/patents

      For more information go to www.QFITLIA.com or call 1-800-745-4447.

      This Instructions for Use has been approved by the US Food and Drug Administration.
      Issued: March 2025

NDC 58468-0348-1
Rx only

Qfitlia™
(fitusiran) injection
50 mg/0.5 mL

For Subcutaneous Use Only

Dispense the enclosed Medication Guide to each patient.

One 0.5 mL Single-Dose Prefilled Pen

sanofi

Principal Display Panel (0.5 mL Syringe Carton)

NDC 58468-0347-1
Rx only

Qfitlia™
(fitusiran) injection
20 mg/0.2 mL

For Subcutaneous Use Only

Dispense the enclosed Medication
Guide to each patient.

One 0.2 mL Single-Dose Vial.
Discard Unused Portion.

sanofi

Principal Display Panel (0.2 mL Vial Carton)