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hympavzi marstacimab injection hemophilia 150mg 1ml

Description

 Indication & Scope

Hympavzi® Marstacimab Injection provides routine prophylaxis to reduce bleeding frequency in patients with hemophilia A or B aged 12 years and older weighing ≥35 kg.

  • Mechanism: Fully human IgG1 monoclonal antibody that specifically binds tissue factor pathway inhibitor (TFPI). It blocks TFPI’s endogenous anticoagulant activity, restores physiological blood coagulation cascade and reduces spontaneous bleeding events without factor replacement.
  • Drug class: Anti-TFPI monoclonal antibody / Hemophilia prophylactic biological agent.
  • Clinical use: Long-term preventive treatment for adolescents and adults with hemophilia A/B, with or without clotting factor inhibitors, to lower annualized bleeding rate.
Specification
Generic Name Marstacimab Injection
Brand Name Hympavzi
Ingredient Marstacimab
Dosage Form Injection
Package 150mg(1ml)*1 syringe/box
Conditions Treated Hemophilia A and Hemophilia B
Taboos Known severe hypersensitivity to marstacimab or any antibody formulation excipients; patients with active unmanaged thromboembolic disorders
Place of origin Rijksweg 12, Puurs-Sint-Amands 2870 BELGIUM
Prescription type Prescription-only
Storage Conditions Sealed prefilled syringes refrigerated at 2°C to 8°C, do not freeze; avoid direct intense light exposure.
Manufacturer Pfizer Inc.
Registration Authority National Medical Products Administration (NMPA), China
Approval number SJ20250026
Approval Date Nov 18, 2025
Shelf Life 30 months

How to use ?

Recommended Dose: Loading dose: 300 mg subcutaneous split into two 150 mg injections on day 1; maintenance dose 150 mg once weekly starting 7 days after loading injection.

 

Time: Weekly subcutaneous injection, fixed same day each week, no meal restriction on timing.

 

Instructions for use: Inject subcutaneously at separate abdominal or thigh sites for loading dose two injections; rotate injection locations weekly; adjust to 300 mg weekly if bleeding control remains insufficient.

 

Interaction: Concurrent activated prothrombin complex concentrates raise thrombotic risk; monitor coagulation markers when combined with bypassing agents for breakthrough bleeds.

 

Side effects:

1. Common: injection site pruritus, headache, mild fever, joint pain, diarrhea, skin rash.

2.Severe rare adverse events: venous or arterial thrombosis, hypersensitivity anaphylaxis.

Important Notice

This product should be administered only by qualified healthcare professionals in accordance with the approved prescribing information and local clinical guidelines. Dosage and administration may vary depending on patient condition, indicatiaon, and regional regulatory requirements.

Packaging & Shipping

Packaging

Original manufacturer’s packaging with secure export carton. Customized export packaging is available upon request.

Shipping Methods

Express Courier (EMS, DHL, FedEx, UPS), Air Freight, and Sea Freight. Cold-chain transportation is available for products requiring temperature-controlled logistics.

Export Support

Certificate of Analysis

GMP Certificate

Commercial Invoice

Packing List & CPP

Cold Chain Logistics

Customs Documentation

Scientific and regulatory sources

1.WHO References
2.NMPA
3.FDA
4.EMA

FAQ

What coagulation protein target does Marstacimab Injection bind to?

It binds tissue factor pathway inhibitor (TFPI) to restore clotting function.

What is the standard maintenance dosing frequency for Marstacimab Injection?

150 mg administered subcutaneously once every week.

What severe adverse risk requires close clinical monitoring during treatment of Marstacimab Injection?

Increased risk of blood clotting and thromboembolic events.

Which patients are not allowed to receive Marstacimab Injection?

Patients with severe allergy to marstacimab or active untreated thrombosis.

Hympavzi® | Marstacimab Injection | Hemophilia | DengYueRX

INN: Marstacimab Injection
Indications: Hemophilia
Dosage Form: Injection
Strength: 150mg(1ml)/syringe

Low MOQ

WHO-GMP

Worldwide Delivery

Compliance and Regulatory Documents

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