|Articles|February 1, 2008

Oncology NEWS International

  • Oncology NEWS International Vol 17 No 2
  • Volume 17
  • Issue 2

FDA reviewing sBLA for Pegintron for melanoma

Schering-Plough Corporation has announced that FDA has granted priority review to its supplemental Biologics License Application for Pegintron (pegylated interferon alfa-2b) as adjuvant therapy for patients with stage III melanoma.

KENILWORTH, New Jersey—Schering-Plough Corporation has announced that FDA has granted priority review to its supplemental Biologics License Application for Pegintron (pegylated interferon alfa-2b) as adjuvant therapy for patients with stage III melanoma. The agent is currently approved for use in the treatment of chronic hepatitis C. The company said that FDA's Oncology Drugs Advisory Committee will discuss the application at its meeting in March.

Articles in this issue

over 18 years ago

NLST article not balanced, critic of screening trial asserts

over 18 years ago

M.D. Anderson and AstraZeneca form neuropathic pain alliance

over 18 years ago

Good nilotinib responses in imatinib-resistant AP-CML

over 18 years ago

Virus linked to Merkel cell carcinoma

over 18 years ago

Benefit of adjuvant RT/CT for pancreatic ca affirmed

over 18 years ago

Recurrence Score helps select node+ pts for chemo

over 18 years ago

For resectable liver mets: Preop chemotherapy or not?

over 18 years ago

Plerixafor boosts stem cell mobilization in myeloma pts

over 18 years ago

MRI shows second-hand smoke damage

over 18 years ago

Assay has high sensitivity for hard-to-detect SLN mets

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