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Study details
Enrolling now

Highly Selective CDK7 Inhibitor Q901 in Advanced Solid Tumors

Qurient Co., Ltd.
NCT IDNCT05394103ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1/2

Target enrollment

130

Study length

about 4 years

Ages

18+

Locations

7 sites in AZ, CA, FL +4

What this study is about

This trial is testing a new drug called Q901, which blocks the activity of CDK7. It's being tested in people with advanced solid tumors who have not responded to other treatments. The goal is to see if Q901 can help shrink or control the cancer and how safe it is.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take KEYTRUDA® (pembrolizumab)
  • 2.Take Q901

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Injection / IV

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

immunotherapy (PD-1 inhibitor immunotherapy (pembrolizumab)), pembrolizumab (Immune checkpoint inhibitor; blocks PD-1 to boost T-cell attack on cancer)

Drug routes

infusion

Endpoints

Primary: Number of participants with treatment-related adverse events as assessed by CTCAE v4.0

Secondary: Change in the area under curve (AUC) of Q901, Change in the maximum plasma concentration (Cmax) of Q901, Change in the time of maximum plasma concentration (Tmax) of Q901