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enzeshu suvemcitug for injection ovarian fallopian tube cancer ppc 50mg

Description

 Indication & Scope

EnZeShu® Suvemcitug for Injection treats adult patients with recurrent ovarian cancer, fallopian tube cancer, or primary peritoneal cancer.

  • Mechanism: It is a monoclonal antibody targeting specific tumor-associated antigens, which binds to tumor cell surface markers, mediates antibody-dependent cellular cytotoxicity and complement-dependent cytotoxicity to eliminate malignant tumor cells.
  • Drug class: Monoclonal antibody anti-tumor agent.
  • Clinical use: First-line or maintenance targeted treatment for recurrent epithelial ovarian, fallopian tube and primary peritoneal malignancies in adults.
Specification
Generic Name Suvemcitug for Injection
Brand Name EnZeShu
Ingredient Suvemcitug
Dosage Form Injection
Package 50mg*1 vial/box
Conditions Treated Recurrent ovarian cancer, recurrent fallopian tube cancer, primary peritoneal cancer in adult population
Taboos Patients with confirmed severe hypersensitivity to Suvemcitug or any auxiliary components of the preparation
Place of origin China
Prescription type Prescription-only
Storage Conditions Store refrigerated at 2°C to 8°C, avoid freezing and direct sunlight
Manufacturer XianSheng Biopharmaceutical, Ltd.
Registration Authority National Medical Products Administration (NMPA), China
Approval number S20250037
Approval Date Jun 30, 2025
Shelf Life 24 months

How to use ?

Recommended Dose: Administer according to body weight; standard dose is given by intravenous infusion once every 3 weeks.

 

Time: Infusion shall be completed within 60–90 minutes, repeated every 21 days as a treatment cycle.

 

Instructions for use: Reconstitute the sterile powder with matching solvent, dilute with normal saline before slow intravenous infusion; premedicate with anti-allergic drugs to prevent infusion reactions.

 

Interaction: No definitive interaction data with chemotherapeutics; concurrent use of other immunotherapies requires close clinical monitoring.

 

Side effects:

1. Common: fatigue, nausea, hypoalbuminemia, infusion-related fever, peripheral edema.

2. Severe: severe anaphylaxis, neutropenia, liver function abnormality.

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 are the main indications of Suvemcitug for Injection?

It is indicated for adult patients with recurrent ovarian cancer, fallopian tube cancer, or primary peritoneal cancer.

What are the common side effects of Suvemcitug for Injection?

Common side effects include fatigue, nausea, hypoalbuminemia, infusion-related fever and peripheral edema.

What is the core anti-tumor mechanism of Suvemcitug for Injection?

It binds to tumor cell surface markers and mediates antibody-dependent cellular cytotoxicity and complement-dependent cytotoxicity to eliminate malignant tumor cells.

Who is prohibited from using Suvemcitug for Injection?

Patients with severe hypersensitivity to Suvemcitug or any auxiliary components of the preparation are contraindicated.

EnZeShu® | Suvemcitug for Injection | Ovarian Cancer/Fallopian Tube Cancer/Primary Peritoneal Cancer | DengYueRX

INN: Suvemcitug for Injection
Indications: Ovarian cancer, fallopian tube cancer, or primary peritoneal cancer
Dosage Form: Injection
Strength: 50mg/vial

Low MOQ

WHO-GMP

Worldwide Delivery

Compliance and Regulatory Documents

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