March 31st 2025
A phase 3 trial plans to further assess neoadjuvant darovasertib for the potential treatment of patients with primary uveal melanoma.
Nivolumab/Relatlimab Shows PFS/OS Benefit Over Nivolumab in Melanoma
May 5th 2023During a Targeted Oncology™ Case-Based Roundtable™ event, Michael B. Atkins, MD, discussed data from the RELATIVITY-047 trial of nivolumab plus relatlimab for patients with metastatic melanoma. This is the second of 2 articles based on this event.
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FDA Type C Meeting Shows Clinical Activity of Darovasertib/Crizotinib in MUM
April 25th 2023Promising results from a type C meeting with the FDA has led to a phase 2/3 trial of darovasertib and crizotinib being initiated in 2023 for patients with first-line HLA-A2 negative metastatic uveal melanoma.
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Efficacy and Tolerability of Immunotherapies Discussed for Melanoma
April 20th 2023During a Targeted Oncology™ Case-Based Roundtable™ event, Michael B. Atkins, MD, discussed with other oncologists what efficacy and safety data aid them in choosing an immunotherapy regimen for patients with metastatic melanoma. This is the first of 2 articles based on this event.
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Clinical Commentary: Tawbi Assesses Toxicities of Therapies in Advanced Melanoma
April 10th 2023During a live webinar, Hussein Tawbi, MD, PhD, discussed first-line therapy for patients with stage IV melanoma, particularly the impact of targeting both PD-1 and LAG3 in these patients by using nivolumab and relatlimab.
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FDA Accepts sBLA of Nivolumab Monotherapy for Stage IIB/IIC Melanoma
February 28th 2023Efficacy findings from CheckMate-76 have led the FDA to accept the supplemental biologics license application and the EMA to validate the type II variation marketing authorization application for nivolumab alone in stage IIB or IIC melanoma.
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FDA Greenlights BTD of a Personalized mRNA Vaccine for High-Risk Melanoma
February 23rd 2023The FDA has granted a breakthrough therapy designation to mRNA-4157/V940 based on data from KEYNOTE-942 which showed that the addition of an mRNA vaccine to adjuvant pembrolizumab improved recurrence-free survival following resection of high-risk melanoma.
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FDA Grants Orphan Drug Designation to LNS8801 for Metastatic Cutaneous Melanoma
January 19th 2023LNS8801 has proven to be safe, well-tolerated, and demonstrated clinical benefit in patients with advanced cancers. Now, the FDA has granted the agent orphan drug designation for metastatic cutaneous melanoma.
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Personalized mRNA Cancer Vaccine Reduces Rate of Recurrence in Melanoma
December 14th 2022A phase 2b trial of pembrolizumab plus a personalized mRNA vaccine resulted in improved recurrence-free survival in patients with resected high-risk melanoma, the first successful randomized trial of its kind.
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LAG-3/PD-1 Inhibitor Therapy in Unresectable or Metastatic Melanoma: The RELATIVITY-047 Trial
November 29th 2022Sajeve Thomas, MD, reflects on the RELATIVITY-047 trial combining relatlimab, a LAG-3 inhibitor, with nivolumab, a PD-1 inhibitor, in the first-line setting of unresectable or metastatic melanoma.
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