Remove clinical ovarian-cancer
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Datopotamab deruxtecan by Daiichi Sankyo for Epithelial Ovarian Cancer: Likelihood of Approval

Pharmaceutical Technology

Datopotamab deruxtecan is under clinical development by Daiichi Sankyo and currently in Phase II for Epithelial Ovarian Cancer.

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Datopotamab deruxtecan by Daiichi Sankyo for Metastatic Ovarian Cancer: Likelihood of Approval

Pharmaceutical Technology

Datopotamab deruxtecan is under clinical development by Daiichi Sankyo and currently in Phase II for Metastatic Ovarian Cancer.

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Farletuzumab ecteribulin by Eisai for Ovarian Cancer: Likelihood of Approval

Pharmaceutical Technology

Farletuzumab ecteribulin is under clinical development by Eisai and currently in Phase II for Ovarian Cancer.

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AbbVie agrees $10 billion oncology acquisition

European Pharmaceutical Review

The antibody-drug conjugate is the first to be approved for platinum-resistant ovarian cancer (PROC) and show meaningful survival benefit for this form of the disease. As such, ongoing clinical development programmes are underway, according to AbbVie.

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Bleeding Problems Prompt FDA Partial Hold on Tests of Mersana Cancer Drug

MedCity News

For the second time in three months, Mersana Therapeutics is dealing with an FDA clinical hold. The partial hold on tests of its experimental ovarian cancer drug follows a full hold placed on an early-stage test of a different Mersana therapy in various types of solid tumors.

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How Data for ImmunoGen Drug Could the Way Doctors Treat Ovarian Cancer

MedCity News

In a confirmatory Phase 3 test of ImmunoGen’s Elahere, the ovarian cancer drug handily beat chemotherapy with results that clinicians say could make the treatment the new standard of care for certain patients. The data were presented during the annual meeting of the American Society of Clinical Oncology.

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EC approves first-line ovarian cancer treatment

European Pharmaceutical Review

The small molecule treatment is indicated as a first-line maintenance treatment for individuals with advanced ovarian cancer regardless of their BRCA mutation status, who have responded to first-line platinum-based chemotherapy. ” The EC based its approval the Phase III ATHENA-MONO study results.