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Study details
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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

About this study

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.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take KEYTRUDA® (pembrolizumab)
  • 2.Take Q901
PhasePhase 1/Phase 2
DrugKEYTRUDA® (pembrolizumab)
Routeinfusion
Primary goalNumber of participants with treatment-related adverse events as assessed by CTCAE v4.0

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low8%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

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