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FDA Approves Accord BioPharma's IMULDOSA (Ustekinumab-srlf) as Biosimilar

9 months ago2 min read

Key Insights

  • Accord BioPharma has received FDA approval for IMULDOSA (Ustekinumab-srlf), a biosimilar to Stelara, used in treating inflammatory diseases.

  • IMULDOSA is approved for multiple indications, including plaque psoriasis, psoriatic arthritis, Crohn's disease, and ulcerative colitis, offering a cost-effective alternative.

  • This approval marks a significant advancement in providing accessible treatment options for patients with chronic inflammatory conditions.

The U.S. Food and Drug Administration (FDA) has approved IMULDOSA (Ustekinumab-srlf), a biosimilar developed by Accord BioPharma referencing Stelara (ustekinumab). This approval marks a significant milestone in providing more accessible and potentially cost-effective treatment options for patients suffering from various inflammatory diseases. IMULDOSA is indicated for the treatment of plaque psoriasis, psoriatic arthritis, Crohn's disease, and ulcerative colitis.

Therapeutic Indications and Clinical Significance

IMULDOSA, like its reference product Stelara, is a human interleukin-12 and interleukin-23 antagonist. It functions by binding to the p40 subunit shared by IL-12 and IL-23, thereby disrupting their interaction with cell surface receptors and inhibiting downstream signaling pathways. This mechanism is crucial in managing the inflammatory responses characteristic of the approved indications.
  • Plaque Psoriasis: Characterized by raised, inflamed, scaly patches, plaque psoriasis affects millions worldwide. IMULDOSA offers a systemic treatment option for patients with moderate-to-severe disease.
  • Psoriatic Arthritis: This chronic, inflammatory arthritis affects both the joints and skin. IMULDOSA can help reduce joint pain, swelling, and stiffness, improving overall physical function.
  • Crohn's Disease: A chronic inflammatory bowel disease (IBD) that causes inflammation of the digestive tract. IMULDOSA is approved for inducing and maintaining remission in adults with moderately to severely active Crohn's disease.
  • Ulcerative Colitis: Another form of IBD, ulcerative colitis causes inflammation and ulcers in the lining of the large intestine and rectum. IMULDOSA is indicated for the treatment of adults with moderately to severely active ulcerative colitis.

Impact and Accessibility

The approval of IMULDOSA as a biosimilar is poised to have a substantial impact on the treatment landscape. Biosimilars are designed to have the same clinical effect as their reference product but are typically offered at a lower cost. This increased accessibility can alleviate the financial burden on patients and healthcare systems, ensuring that more individuals can receive necessary treatment.
Accord BioPharma's IMULDOSA represents a valuable addition to the therapeutic armamentarium for inflammatory diseases, offering a new option for patients and healthcare providers alike.
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