Genmab (Otc) ((GMAB)) announced an update on their ongoing clinical study.
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Genmab has initiated a Phase 3 clinical study titled ‘A Phase 3 Randomized, Open-label Study of Rinatabart Sesutecan (Rina-S) Versus Treatment of Investigator’s Choice (IC) in Patients With Endometrial Cancer After Platinum-Based Chemotherapy and PD(L)-1 Therapy.’ The study aims to evaluate the efficacy and safety of Rina-S compared to standard treatments like paclitaxel or doxorubicin in patients with recurrent or progressive endometrial cancer. This research is significant as it seeks to improve treatment options for patients who have undergone prior therapies.
The study tests Rina-S, an experimental drug administered via intravenous infusion every three weeks. It is compared against standard chemotherapy options chosen by the investigator, either paclitaxel or doxorubicin, both delivered through IV methods.
This interventional study is randomized and follows a parallel assignment model with no masking, focusing primarily on treatment. Participants have a 50:50 chance of receiving either Rina-S or a standard chemotherapy agent, with the study expected to last approximately three years.
The study is not yet recruiting, with key dates including a submission on September 9, 2025, and the last update on October 23, 2025. These dates are crucial as they mark the beginning of the study’s timeline and its latest developments.
The market implications of this study are significant for Genmab’s stock performance, as successful results could enhance investor confidence and position the company as a leader in endometrial cancer treatment. This update may also influence the competitive landscape, particularly among companies focusing on oncology therapies.
The study is ongoing, with further details available on the ClinicalTrials portal.