Celgene Corp. (NASDAQ: CELG) saw its shares take a step back early Friday after the firm announced in conjunction with the Lymphoma Study Association (LYSA) the results from a late-stage clinical study. The study evaluated Revlimid plus rituximab in patients with previously untreated follicular lymphoma.
Specifically, this investigational study evaluated Revlimid plus rituximab (R²) followed by (R²) maintenance compared to the standard of care with rituximab plus chemotherapy (R-CHOP, R-bendamustine or R-CVP) followed by rituximab maintenance in patients with previously untreated follicular lymphoma.
The rituximab treatment arm did not achieve superiority in the co-primary endpoints of complete response or unconfirmed complete response (CR/CRu) at 120 weeks and progression-free survival (PFS) during the pre-planned analysis (final analysis of CR/CRu and interim analysis of PFS). Neither arm was superior for either of the co-primary endpoints.
The safety findings were consistent with the known profiles of the regimens investigated. There are additional analyses that are ongoing and planned.
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Prof. Gilles Salles, President of LYSA, added:
This is the first Phase III trial to evaluate a chemotherapy-free regimen to the established standard of care in patients with previously untreated follicular lymphoma and represents a landmark study in this disease setting. We look forward to further analyzing and presenting these important data at a future medical congress.
Excluding Friday’s move, Celgene had underperformed the broad markets, with its stock down about 7% year to date. Over the past quarter, the stock was down about 25%.
Shares of Celgene were down over 3% at $104.24 Friday morning, with a consensus analyst price target of $124.59 and a 52-week range of $94.55 to $147.17.
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