GNH USA

Europe — EMA

Jemperli

GNH USA supplies Jemperli (Dostarlimab), a monoclonal antibody PD‑1 inhibitor for dMMR/MSI‑H advanced or recurrent endometrial cancer.

Dostarlimab

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What is Dostarlimab?

Dostarlimab, the active ingredient in Jemperli, is a monoclonal antibody presented as a lyophilized powder for solution for infusion for intravenous use. It treats dMMR/MSI‑H advanced or recurrent endometrial cancer in adult patients.

GNH USA supplies Jemperli as a licensed, GDP-compliant international pharmaceutical supplier serving oncology centres worldwide.

What is Dostarlimab used for?

Jemperli is a PD‑1 inhibitor used in the management of cancers that exhibit deficient mismatch repair or high microsatellite instability.

- dMMR/MSI‑H advanced or recurrent endometrial cancer: improves disease control in patients whose tumors show these biomarkers. - Endometrial cancer (PD‑1 inhibitor therapy): provides an immunotherapy option for patients with specific molecular profiles. - Microsatellite instability‑high solid tumours (investigational): being evaluated in clinical studies for broader oncologic use.

What are the side effects of Dostarlimab?

Jemperli may cause a range of immune‑related adverse reactions.

Common Side Effects: - Fatigue: persistent tiredness reported by many patients. - Nausea: mild to moderate gastrointestinal upset. - Diarrhoea: loose stools that may require supportive care. - Rash or pruritus: skin irritation or itching. - Infusion‑related reactions: transient fever, chills, or flushing during administration.

Serious or Rare Side Effects: - Immune‑mediated pneumonitis: inflammation of lung tissue that can be life‑threatening. - Colitis or hepatitis: severe inflammation of the colon or liver requiring immunosuppression. - Endocrinopathies: thyroiditis, adrenal insufficiency, or hypophysitis. - Severe infusion reactions: anaphylaxis or cardiovascular compromise. - Myocarditis: inflammation of heart muscle with potential cardiac dysfunction.

What precautions apply to Dostarlimab?

When using Jemperli, clinicians should observe several safety measures.

- Monitor for immune‑mediated adverse events: assess organ function regularly. - Manage infusion reactions: have emergency medications and monitoring equipment ready. - Avoid live vaccines: immunosuppression may reduce vaccine efficacy. - Pregnancy and breastfeeding: safety not established; weigh potential risks and benefits. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Dostarlimab interact with?

Jemperli can interact with other therapies that affect the immune system.

Major Interactions (Avoid): - Concurrent use with other PD‑1/PD‑L1 inhibitors: increased risk of severe immune toxicity. - Combination with systemic immunosuppressants: may diminish therapeutic efficacy. - Live vaccines: heightened risk of infection due to immune modulation.

Moderate Interactions (Monitor Closely): - Corticosteroids: may mask signs of immune‑related adverse events. - Anticoagulants: monitor for bleeding if thrombocytopenia develops. - Enzyme‑inducing drugs: no known pharmacokinetic effect but clinical response should be observed.

Frequently asked questions

What is Jemperli used for?+
Jemperli (dostarlimab) is indicated for the treatment of adult patients with advanced or recurrent endometrial cancer that is deficient in mismatch repair (dMMR) or exhibits high microsatellite instability (MSI‑H). It provides an immunotherapy option by targeting the PD‑1 pathway to enhance anti‑tumour immune responses.
How does Dostarlimab work?+
Dostarlimab is a monoclonal antibody that binds to the PD‑1 receptor on T cells, blocking its interaction with PD‑L1 and PD‑L2. This interruption lifts the inhibitory checkpoint, allowing T cells to recognise and attack cancer cells more effectively, thereby restoring immune‑mediated tumour control.
What is the usual dose of Jemperli?+
The dosing regimen for Jemperli is determined by the prescribing oncologist based on the patient’s clinical condition, body weight, and treatment protocol. The prescriber sets the infusion schedule and any dose adjustments required during therapy.
Is Jemperli safe during pregnancy or breastfeeding?+
Safety of Jemperli in pregnancy or while breastfeeding has not been established. The drug may pose risks to the fetus or infant, so it should only be used if the potential benefit justifies the potential harm. Consultation with a specialist is essential before exposure.
How do I order Jemperli from GNH USA?+
To order Jemperli, submit an enquiry on the product page at gnh-usa.com specifying the required quantity. GNH USA supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, cold‑chain shipping details and necessary import documentation.
How does Jemperli compare with other PD‑1 inhibitors?+
Jemperli (dostarlimab) belongs to the same class as pembrolizumab and nivolumab, sharing the PD‑1 blockade mechanism. Clinical data suggest comparable efficacy in dMMR/MSI‑H tumours, though differences may exist in dosing intervals, safety profiles, and regulatory approvals across regions.
What are the storage and handling requirements for Jemperli?+
Jemperli is supplied as a lyophilized powder for infusion and must be stored refrigerated at 2‑8 °C. It should be kept in its original packaging, protected from light, and must not be frozen or shaken before reconstitution.
How is Jemperli administered?+
Jemperli is administered intravenously. The lyophilized powder is reconstituted with a suitable diluent to create a solution for infusion, which is then delivered over a prescribed period under medical supervision, typically in an oncology infusion centre.
What are the most serious risks to watch for while on Jemperli?+
Serious risks include immune‑mediated pneumonitis, colitis, hepatitis, endocrinopathies (such as thyroiditis), severe infusion reactions, and myocarditis. Patients should be monitored closely for symptoms like persistent cough, abdominal pain, jaundice, hormonal changes, or cardiac discomfort, and managed promptly.
Who should not use Jemperli?+
Jemperli should not be used in patients with known hypersensitivity to dostarlimab or any of its excipients. It is also contraindicated in individuals receiving other PD‑1/PD‑L1 inhibitors concurrently, and caution is advised for patients with active autoimmune diseases or uncontrolled infections.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Dostarlimab
Route
Intravenous Use
Manufacturer
Glaxosmithkline (Ireland) Limited
Origin
EU

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