HomeNewsBusinessStocksCipla closes in on 52-week high on getting USFDA nod for cancer drug

Cipla closes in on 52-week high on getting USFDA nod for cancer drug

According to external data that Cipla provided, Revlimid (Lenalidomide) capsules had US sales of approximately $2.58 billion for the 12-month period ending June 2022

September 07, 2022 / 14:47 IST
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Shares of Cipla gained on September 7 after the drug maker announced that it received the final approval from the US drug regulator to launch the generic version of a rare blood cancer medicine.

The United States Food and Drug Administration (US FDA) had approved its Abbreviated New Drug Application (ANDA) for Lenalidomide capsule 5 mg, 10 mg, 15 mg and 25 mg, the pharma company said in a regulatory filing.

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Cipla’s Lenalidomide Capsules are AB-rated therapeutic equivalent generic versions of Bristol Myers Squibb’s (Celgene) Revlimid (Lenalidomide) Capsules.

Lenalidomide is used in the treatment of multiple myeloma, a cancer of plasma cells. Apart from that, the immunomodulatory prescription drug, which suppresses the immune system, is indicated for several other blood- related malignancies in adults such as myelodysplastic syndromes, mantle cell lymphoma, follicular lymphoma and marginal zone lymphoma.