NATCO Pharma Launches Generic Blood Cancer Treatment Medicine in US
Natco Pharma announced the launch of generic Pomalidomide capsules indicated for treatment of adult patients with blood and bone marrow cancer in the US market in partnership with Breckenridge Pharmaceutical, Inc.
Pomalidomide capsule is a generic version of Pomalyst by Celgene.
The product is available in 1mg, 2mg, 3mg, and 4mg strengths and is distributed primarily through specialty pharmacies and clinics, Natco Pharma said in a regulatory filing.
Vice Chairman and CEO Rajeev Nannapaneni says, “This further strengthens our oncology and specialty portfolio in the US. The launch highlights our commitment to our mission of making specialty medicines accessible to all the patients worldwide."
Breckenridge Pharmaceutical, Inc President and Chief Commercial Officer, Brian Guy says, "We look forward to bringing more such complex and specialty products to the market in the coming years. Breckenridge's launch of Pomalidomide capsules delivers a high-quality, affordable generic solution is supported by copay assistance for eligible patients to help reduce treatment delays and ensure continuity of care. Access and affordability continue to be major challenges for patients who depend on specialty therapies.”
Also Read: 5 Latest CHRO Appointments in Global Corporations
Natco Pharma said Pomalidomide capsules are indicated for treatment of adult patients with multiple myeloma who have received at least two prior therapies, including lenalidomide and a proteasome inhibitor and have demonstrated disease progression on or within 60 days of completion of the last therapy.
Also Read: A Brief History of India's Transformation Under PM Narendra Modi
It is also approved for AIDS-related Kaposi sarcoma after failure of highly active antiretroviral therapy, as well as for HIV-negative adult patients with Kaposi sarcoma, the company added.
Pomalidomide Capsules, 1mg, 2mg, 3mg and 4mg, had estimated sales of $ 3.2 billion in the US for 12 months ended September 2025 as per industry sales data, it said.
Also Read: How This Techie Turned Visa Struggles into Startup Success
Natco believes based on information made available by the US Food and Drug Administration (FDA), it has 180 days of shared exclusivity for marketing the drug.