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Study identifier: NCT07024784 Synced from ClinicalTrials.gov · July 28, 2026
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A Study to Assess Change in Disease Activity and Adverse Events in Adult Participants With Gynecologic Cancers Receiving Intravenous Infusion of IMGN151 as Monotherapy or in Combination With Other Therapies

Condition: Gynecologic Cancers · Platinum-Sensitive Ovarian Cancer · Fallopian Tube Cancer  ·  Sponsor: AbbVie

PhasePhase 2
Planned participants377
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

Cancer is a condition where cells in a specific part of body grow and reproduce uncontrollably. The purpose of this study is to assess safety and tolerability of IMGN151 when given as monotherapy and in combination with other anti-cancer therapies in adult participants with gynecologic cancers. IMGN151 is an investigational drug being developed for the treatment of gynecologic cancers. Participants are placed in 1 of 4 groups, called treatment arms. Each group receives a different treatment. Around 377 participants with gynecologic cancers will be enrolled in the study at approximately 50 sites worldwide. Participants will receive intravenous infusions of IMGN151 as monotherapy or in combination with anti-cancer therapies according to their assigned study arm. In Arm A, participants will receive IMGN151 in combination with carboplatin on Day 1 of each cycle. In Arm B, participants will receive IMGN151 in combination with olaparib, twice a day (BID) on Day 1 of each cycle. In Arm C, participants will receive IMGN151 in combination with bevacizumab on Day 1 of each cycle. In Arm D, participants will receive IMGN151 as monotherapy on Day 1 of each cycle. In Arm E, participants will receive IMGN151 as monotherapy on Day 1 of each cycle. In Arm F, participants will receive IMGN151 as monotherapy on Day 1 of each cycle. The total study duration will be approximately 3 years. There may be higher treatment burden for participants in this trial compared to their standard of care. P…

This description comes directly from the study's public registry record.

Talk to the study team

ABBVIE CALL CENTER  ·  844-663-3742  ·  abbvieclinicaltrials@abbvie.com

Always discuss trial participation with your own doctor first.

Locations (16)

Holy Name Medical Center /ID# 279017Teaneck, New Jersey, United StatesRecruiting
University of Cincinnati Medical Center. /ID# 278925Cincinnati, Ohio, United StatesRecruiting
OU Health - Stephenson Cancer Center /ID# 277656Oklahoma City, Oklahoma, United StatesRecruiting
Providence Portland Medical Center /ID# 277727Portland, Oregon, United StatesRecruiting
Women & Infants Hospital /ID# 277930Providence, Rhode Island, United StatesRecruiting
SCRI Oncology Partners /ID# 279733Nashville, Tennessee, United StatesRecruiting
Texas Oncology-Austin North /ID# 279958Austin, Texas, United StatesRecruiting
Next Virginia /ID# 279684Fairfax, Virginia, United StatesRecruiting
Rabin Medical Center /ID# 279142Petah Tikva, Central District, IsraelRecruiting
The Chaim Sheba Medical Center /ID# 275997Ramat Gan, Tel Aviv, IsraelRecruiting
Tel Aviv Sourasky Medical Center /ID# 275852Tel Aviv, Tel Aviv, IsraelRecruiting
Rambam Health Care Campus- Haifa /ID# 276004Haifa, IsraelRecruiting

+ 4 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT07024784