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Study identifier: NCT07335497 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

CR-001 in Adult Participants With Locally Advanced or Metastatic Solid Tumors

Condition: Locally Advanced / Metastatic Solid Tumors  ·  Sponsor: Crescent Biopharma, Inc.

PhasePhase 1/Phase 2
Planned participants290
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The purpose of this study is to determine the safety and tolerability of monotherapy CR-001 and identify the maximum tolerated dose (MTD), and/or optimal biologic dose and Recommended Phase 2 Dose(s) (RP2D) in participants with locally advanced or metastatic solid tumors.

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

Talk to the study team

Crescent Clinical Trials  ·  617-430-5595  ·  clinicaltrials@crescentbiopharma.com

Always discuss trial participation with your own doctor first.

Locations (25)

Clinical Study SiteBirmingham, Alabama, United StatesRecruiting
Clinical Study SiteLos Angeles, California, United StatesRecruiting
Clinical Study SiteDenver, Colorado, United StatesRecruiting
Clinical Study SiteOrlando, Florida, United StatesRecruiting
Clinical Study SiteSarasota, Florida, United StatesRecruiting
Clinical Study SiteDetroit, Michigan, United StatesRecruiting
Clinical Study SiteGrand Rapids, Michigan, United StatesRecruiting
Clinical Study SiteNew York, New York, United StatesRecruiting
Clinical Study SiteColumbus, Ohio, United StatesRecruiting
Clinical Study SitePittsburgh, Pennsylvania, United StatesRecruiting
Clinical Study SiteNashville, Tennessee, United StatesRecruiting
Clinical Study SiteDallas, Texas, United StatesRecruiting

+ 13 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT07335497