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AbbVie’s IMGN151 Study: A New Hope for Recurrent Gynecological Cancers

AbbVie’s IMGN151 Study: A New Hope for Recurrent Gynecological Cancers

Abbvie ((ABBV)) announced an update on their ongoing clinical study.

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AbbVie is currently conducting a Phase 1 clinical study titled ‘A Phase 1, First-in-Human, Open-Label, Dose-Escalation and Expansion Study of IMGN151 (Anti-FRα Antibody-drug Conjugate) in Adult Patients With Recurrent Gynaecological Cancers.’ The study aims to evaluate the safety, tolerability, pharmacokinetics, immunogenicity, and preliminary antitumor activity of IMGN151 in patients with various recurrent gynecological cancers. This research is significant as it explores a novel treatment option for patients who are suitable for nonplatinum single-agent therapy.

The intervention being tested is IMGN151, an experimental antibody-drug conjugate (ADC) administered via intravenous infusion every three weeks. Its purpose is to target and treat recurrent gynecological cancers, potentially offering a new line of therapy for patients.

The study follows an interventional design with a sequential intervention model and no masking, focusing primarily on treatment. This design allows for the systematic evaluation of IMGN151’s effects on the targeted conditions.

The study began on August 23, 2022, with an estimated primary completion date yet to be announced. The most recent update was submitted on August 21, 2025. These dates are crucial as they mark the progress and ongoing nature of the study, which is still in the recruiting phase.

From a market perspective, this study’s progress could influence AbbVie’s stock performance and investor sentiment, particularly if the results demonstrate positive outcomes. The development of IMGN151 could position AbbVie competitively within the pharmaceutical industry, especially in the niche market of gynecological cancer treatments.

The study is ongoing, and further details can be accessed on the ClinicalTrials portal.

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