GNH USA

Europe — EMA

Jemperli

GNH USA supplies Jemperli (Dostarlimab), a PD‑1 inhibitor for advanced dMMR endometrial cancer and related solid tumours. Request a quote for global supply.

Dostarlimab

Request sourcing

1
Pack/s

What is Dostarlimab?

Dostarlimab, the active ingredient in Jemperli, is a PD‑1 inhibitor presented as a sterile solution for intravenous infusion. It is used to treat certain advanced endometrial cancers and other mismatch‑repair‑deficient solid tumours 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 indicated for cancers that exhibit mismatch repair deficiency.

- Endometrial cancer (dMMR): improves progression‑free survival in adults with advanced disease. - Solid tumours with high microsatellite instability (MSI‑H): offers an immunotherapy option for patients with MSI‑H tumours. - Recurrent or metastatic endometrial carcinoma: provides treatment when standard therapies have failed.

What are the side effects of Dostarlimab?

Common Side Effects: - Fatigue: persistent tiredness experienced during treatment. - Nausea: mild to moderate feeling of sickness. - Diarrhoea: loose stools occurring intermittently. - Infusion‑related reactions: redness, itching, or fever during administration. - Rash: skin eruptions of varying intensity. - Hypothyroidism: reduced thyroid hormone production.

Serious or Rare Side Effects: - Immune‑mediated colitis: inflammation of the colon requiring urgent care. - Pneumonitis: lung inflammation that may cause breathing difficulties. - Hepatitis: liver inflammation with elevated enzymes. - Severe skin reactions: such as Stevens‑Johnson syndrome. - Endocrinopathies: including adrenal insufficiency. - Myocarditis: inflammation of heart muscle, potentially life‑threatening.

What precautions apply to Dostarlimab?

Before initiating therapy, evaluate patient history and baseline labs. - Monitor for immune‑related adverse events: watch for signs of organ inflammation. - Assess thyroid function: test TSH and free T4 prior to and during treatment. - Screen for hepatitis B/C: test serology to prevent reactivation. - Avoid live vaccines: immunosuppression may increase infection risk. - Pregnancy and lactation: discuss potential risks and consider alternatives. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Dostarlimab interact with?

Dostarlimab may interact with other agents that affect immune function.

Major Interactions (Avoid): - Concurrent use of other immune checkpoint inhibitors: may amplify immune toxicity. - High‑dose systemic steroids or other strong immunosuppressants: can reduce therapeutic efficacy.

Moderate Interactions (Monitor Closely): - Live vaccines: increased risk of infection; schedule appropriately. - Anticoagulants: monitor for bleeding if thrombocytopenia occurs. - CYP450 substrates: generally minimal effect, but observe for unexpected changes.

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 mismatch‑repair deficient, as well as for other solid tumours that display high microsatellite instability. It works as an immunotherapy to help the immune system target cancer cells.
How does Dostarlimab work?+
Dostarlimab is a monoclonal antibody that blocks the PD‑1 receptor on T cells, preventing its interaction with PD‑L1 and PD‑L2 on tumour cells. This blockade restores T‑cell activity, allowing the immune system to recognise and destroy cancer cells that would otherwise evade immune detection.
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. Healthcare professionals set the dose and schedule according to approved guidelines and individual patient factors.
Is Jemperli safe during pregnancy or breastfeeding?+
Safety of Jemperli in pregnancy or while breastfeeding has not been established. Women of child‑bearing potential should be advised of potential risks and use effective contraception. Breastfeeding decisions should be made after discussing possible effects with a healthcare provider.
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 works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if needed), and 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 target. Clinical data suggest comparable efficacy in dMMR tumours, with a safety profile consistent with the class. Choice among agents often depends on regulatory approval, dosing schedule, and individual patient considerations.
What are the storage and handling requirements for Jemperli?+
Jemperli must be stored refrigerated at 2‑8 °C. Keep the vials in the original packaging, protect them from light, and avoid freezing or shaking. If temporary storage at room temperature is unavoidable, limit exposure to no more than 30 minutes before administration.
How is Jemperli administered?+
Jemperli is supplied as a sterile solution for intravenous infusion. It is administered by a qualified healthcare professional, typically over a period of 30 minutes to one hour, following the dosing schedule prescribed by the treating oncologist.
What are the most serious risks to watch for while on Jemperli?+
Serious risks include immune‑mediated adverse events such as colitis, pneumonitis, hepatitis, severe skin reactions, endocrinopathies, and myocarditis. Patients should be monitored closely for symptoms like persistent diarrhea, shortness of breath, jaundice, rash, or unexplained fatigue and report them promptly.
Who should not use Jemperli?+
Jemperli is contraindicated in patients with known hypersensitivity to dostarlimab or any of its excipients. It should also be avoided in individuals receiving other immune checkpoint 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

Related products