Historically, the median overall survival of metastatic melanoma patients was less than 1 year and long-term survivors were rare. Recent advances in therapies have dramatically shifted this landscape...
BMS has announced positive results from a Phase II trial (CheckMate -069), evaluating the Opdivo (nivolumab)+Yervoy (ipilimumab) regimen versus Yervoy...
BMS announced positive results of a Phase III trial (CheckMate -067) evaluating the Opdivo (nivolumab)+Yervoy (ipilimumab) regimen or Opdivo monotherapy...
BMS announced that the FDA has accepted for filing and review a supplemental Biologics License Application (sBLA) for the combination...
Bristol-Myers Squibb announced that the FDA approved Opdivo (nivolumab) in combination with Yervoy (ipilimumab), for the treatment of patients with...
This ASCO guideline update reviews systemic therapy for melanoma, adding new recommendations for neoadjuvant pembrolizumab, adjuvant nivolumab or pembrolizumab, and combination regimens for advanced disease. It also removes outdated options like talimogene laherparepvec.
The EMA has validated the application from BMS for Opdivo (nivolumab) + Yervoy (ipilimumab) to treat melanoma, the proposed new...
Bristol-Myers Squibb announced that the European Commission (EC) has approved Opdivo + Yervoy (nivolumab + ipilimumab) for the treatment of...
Bristol Myers Squibb announced 10-year follow-up data from CheckMate -067, a randomized, double-blind, Phase III clinical trial, which showed continued durable improvement in survival with first-line Opdivo (nivolumab) plus Yervoy (ipilimumab) therapy and Opdivo monotherapy, versus Yervoy alone, in patients with previously untreated advanced or metastatic melanoma
This randomized phase II trial compares the efficacy of nivolumab alone versus nivolumab combined with ipilimumab in treating recurrent or persistent ovarian cancer. The study finds that the combination therapy significantly improves response rates and progression-free survival compared to nivolumab alone.