FDA approved CAMCEVI ETM long-acting injectable formulation for advanced prostate cancer
“The approval of CAMCEVI ETM (21 mg) is a significant step toward our mission in improving the standard of care and the lives of patients,” said Dr. Ben Chien, founder, Chairman, and CEO of Foresee. “It is also a key step in our efforts to build Foresee as a profitable and growing business. We want to thank the team and all stakeholders for their tireless work, which has made this approval possible.
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