GNH USA

Europe — EMA

Imnovid

GNH USA supplies Imnovid (Pomalidomide), an immunomodulatory antineoplastic for relapsed/refractory multiple myeloma. Request a quote for global supply.

Pomalidomide

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What is Pomalidomide?

Pomalidomide, the active ingredient in Imnovid, is an immunomodulatory agent presented as an oral tablet for oral use. It is indicated for the treatment of relapsed/refractory multiple myeloma in adult patients who have received prior therapies. GNH USA supplies Imnovid as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres worldwide.

What is Pomalidomide used for?

Imnovid is an immunomodulatory drug used in the management of plasma‑cell malignancies, specifically multiple myeloma. - Relapsed/refractory multiple myeloma: improves disease control and extends progression‑free survival when used after prior therapies.

What are the side effects of Pomalidomide?

Adverse reactions to pomalidomide can vary in frequency and severity.

Common Side Effects: - Neutropenia: reduced neutrophil count increasing infection risk. - Anemia: lowered red blood cell levels causing fatigue. - Fatigue: general feeling of tiredness. - Constipation: difficulty passing stools. - Nausea: upset stomach and urge to vomit. - Infections: heightened susceptibility to bacterial or viral infections.

Serious or Rare Side Effects: - Thromboembolic events: blood clots in veins or arteries. - Severe rash or skin reactions: including Stevens‑Johnson syndrome. - Elevated liver enzymes: indicating hepatic stress. - Secondary primary malignancies: emergence of new cancers. - Deep vein thrombosis or pulmonary embolism. - Severe neutropenia leading to febrile neutropenia.

What precautions apply to Pomalidomide?

Before initiating therapy, clinicians should assess patient risk factors and monitor for potential complications. - Blood count monitoring: perform regular CBC to detect neutropenia or anemia. - Thromboembolic risk assessment: evaluate history of clotting disorders and consider prophylactic anticoagulation. - Pregnancy avoidance: enforce strict contraception for women of child‑bearing potential. - Hepatic function evaluation: check liver enzymes prior to and during treatment. - Drug‑specific warnings: avoid concomitant use with known teratogens. - Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

What does Pomalidomide interact with?

Pomalidomide may interact with several drug classes, requiring careful management.

Major Interactions (Avoid): - Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase pomalidomide exposure. - Teratogenic agents: concurrent use can heighten fetal risk. - Immunosuppressants (e.g., high‑dose steroids): may amplify infection risk.

Moderate Interactions (Monitor Closely): - CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce efficacy. - Anticoagulants (e.g., warfarin, DOACs): monitor for altered clotting parameters. - CYP1A2 inhibitors (e.g., fluvoxamine): may modestly increase levels. - Vaccines: live vaccines should be avoided during therapy.

Frequently asked questions

What is Imnovid used for?+
Imnovid contains pomalidomide and is prescribed for adults with relapsed or refractory multiple myeloma who have previously received at least two other therapies. It helps control disease progression and can extend the time before the cancer worsens.
How does pomalidomide work?+
Pomalidomide binds to the cereblon protein, altering the activity of an E3 ubiquitin ligase complex. This leads to degradation of specific transcription factors, reducing cytokine production, inhibiting new blood‑vessel formation, and triggering programmed cell death in malignant plasma cells while enhancing immune‑mediated tumor clearance.
What is the usual dose of Imnovid?+
The dosage of Imnovid is individualized by the prescribing physician based on the patient’s clinical status, prior therapies, and laboratory values. The prescriber determines the appropriate strength, schedule, and any necessary dose adjustments.
Is Imnovid safe during pregnancy or breastfeeding?+
Pomalidomide is classified as a teratogenic agent and is contraindicated in pregnancy. Women of child‑bearing potential must use effective contraception before, during, and after treatment. Safety during breastfeeding has not been established, and nursing is generally discouraged while on therapy.
How do I order Imnovid from GNH USA?+
To place an order, submit an enquiry on the Imnovid 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 any cold‑chain requirements), and necessary import documentation.
How does Imnovid compare with other treatments for multiple myeloma?+
Imnovid (pomalidomide) belongs to the immunomodulatory drug class, similar to lenalidomide and thalidomide, but it is typically used after those agents have failed. It offers a distinct potency profile and may be effective in patients with disease that is refractory to earlier IMiDs, providing an additional therapeutic option.
What are the storage requirements for Imnovid?+
Imnovid tablets should be stored at ambient temperature, below 25 °C, in the original packaging to protect them from moisture and light. Keep the container tightly closed and out of reach of children.
How is Imnovid administered?+
Imnovid is taken orally, usually once daily on a prescribed schedule (e.g., 21 days on, 7 days off). The tablets should be swallowed whole with water and taken at the same time each day, unless the prescriber advises otherwise.
What are the most serious risks associated with Imnovid?+
The most serious risks include severe neutropenia leading to infection, thromboembolic events such as deep‑vein thrombosis or pulmonary embolism, and rare but severe skin reactions. Patients should be monitored closely for signs of infection, clotting, or unusual skin changes.
Who should not use Imnovid?+
Imnovid should not be used by individuals who are pregnant, have uncontrolled infections, have a history of severe thromboembolic disease without appropriate prophylaxis, or have known hypersensitivity to pomalidomide or any excipients in the formulation.
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
Pomalidomide
Route
Oral Use
Manufacturer
Bristol-Myers Squibb Pharma Eeig
Origin
EU

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