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Study identifier: NCT05394103 Synced from ClinicalTrials.gov · August 10, 2026
● Study status: Recruiting

Highly Selective CDK7 Inhibitor Q901 in Selected Advanced Solid Tumors

Condition: Advanced Cancer · Metastatic Cancer  ·  Sponsor: Qurient Co., Ltd.

PhasePhase 1/Phase 2
Planned participants130
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNoCheck eligibility criteria ↓
Where11 locations · 2 countries

Interested? Contact the study team ↓

For sponsors, CROs & site teams
Professional view of this study — listed sites, countries and recruiting context from the public registry. Everything below is written for patients and caregivers.See where this study is running →

About this study

Multicenter, open-label, dose-escalation, safety, tolerability, PK and pharmacodynamic study with a dose expansion at the RP2D to evaluate safety and potential antitumor activity of Q901 as a monotherapy and in combination with pembrolizumab

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

Talk to the study team

Qurient Clinical Trial Information  ·  +82-31-8060-1610  ·  clinicaltrial_info@qurient.com

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: * Participants with histologically or cytologically confirmed advanced or metastatic ovarian, CRPC, HR+ HER2- breast, endometrial, colorectal, small-cell lung, or pancreatic cancer, who have progressed following standard-of-care therapy or for whom there is no standard therapy that confers clinical benefit * Measurable disease per RECIST v 1.1 * ECOG performance status 0,1 or 2 * Life expectancy of at least 3 months * Age ≥ 18 years * Signed, written IRB-approved informed consent form Exclusion Criteria: * New York Heart Association Class III or IV cardiac disease, or myocardial infarction, severe unstable angina, coronary/peripheral artery bypass graft, congestive heart failure within the past 6 months * Have a corrected QT interval (using Fridericia's correction formula) (QTcF) of \>470 msec (females) and \>450 msec (males) * Active, uncontrolled bacterial, viral, or fungal infections, requiring systemic therapy * Active, poorly controlled autoimmune or inflammatory diseases

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (11)

Mayo ClinicPhoenix, Arizona, United StatesRecruiting
University of Southern CaliforniaLos Angeles, California, United StatesRecruiting
Mayo ClinicJacksonville, Florida, United StatesRecruiting
Northwestern UniversityChicago, Illinois, United StatesRecruiting
Mayo ClinicRochester, Minnesota, United StatesRecruiting
Atlantic Health System HospitalMorristown, New Jersey, United StatesRecruiting
Mary Crowley Cancer ResearchDallas, Texas, United StatesRecruiting
National Cancer CenterGoyang-si, South KoreaRecruiting
CHA University Bundang Medical CenterSeongnam-si, South KoreaRecruiting
Asan Medical CenterSeoul, South KoreaNot Yet Recruiting
Severance HospitalSeoul, South KoreaNot Yet Recruiting

More studies in these areas

This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.

PhoenixLos AngelesJacksonvilleChicago

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