At a glance
- What the study gets you
- Access to the study treatment being tested
- Type of study
- Interventional (receives a drug or procedure)
- Time in hospital
- In-person visits at study sites — visit count not specified by the sponsor
- Drug or intervention
- rezatapopt (drug), pembrolizumab (drug)
- How long the study runs
- Study runs about 86 months (dates as stated)
- About the drug or intervention
- rezatapopt — drug: First-in-class, oral, small molecule p53 reactivator selective for the TP53 Y220C mutation. · pembrolizumab — drug: Participants receive pembrolizumab 200 mg by intravenous (IV) infusion over 30 minutes.
- Patient visit burden
- Not specified by the sponsor
- Type of study
- Testing a treatment
- Ages
- 12 Years and over
- Who
- All
- Number of participants
- 300
- Started
- 2020-10-29
- Last checked
- 2026-10
Plain English Summary
What is this study?
- • Testing a new treatment for advanced solid tumor
- • Phase1/Phase2 - 300 participants
- • The Phase 2 monotherapy portion of this study is currently enrolling and will evaluate the efficacy and safety of PC14586 (INN rezatapopt) in participants with locally advanced or metastatic solid tumors harboring a TP53 Y220C mutation
Who can take part?
- • Ages 12 Years and over
- • Diagnosed with advanced solid tumor
Where?
- • London - Sarah Cannon Research Institute UK
- • Newcastle upon Tyne - Freeman Hospital
This is a simplified summary. Always discuss with your doctor before making any decisions.
About This Trial
The Phase 2 monotherapy portion of this study is currently enrolling and will evaluate the efficacy and safety of PC14586 (INN rezatapopt) in participants with locally advanced or metastatic solid tumors harboring a TP53 Y220C mutation. The Phase 1 portion of the study will assess the safety, tolerability and preliminary efficacy of multiple dose levels of rezatapopt as monotherapy and in Phase 1b in combination with pembrolizumab.
More detail
Rezatapopt is a first-in-class, oral, small molecule p53 reactivator that is selective for the TP53 Y220C mutation. The primary objective of Phase 2 Monotherapy is to evaluate the efficacy of rezatapopt at the Recommended Phase 2 Dose (RP2D) including the Overall Response Rate (ORR) in the Ovarian Cancer Cohort and the ORR across all cohorts as determined by blinded independent central review. Secondary objectives of Phase 2 are to characterize the safety, pharmacokinetic (PK) properties, quality of life, and other efficacy measures of PC14586 rezatapopt at the RP2D. Enrollment is open for the Phase 2 Monotherapy portion of the study. The primary objective of Phase 1 Monotherapy is to establish the maximum tolerated dose (MTD) and RP2D of rezatapopt. Secondary objectives are to characterize the PK properties, safety and tolerability, and to assess preliminary efficacy including ORR. Enrollment into Phase 1 Monotherapy is complete. The primary objective of Phase 1b Combination Therapy is to establish the MTD/RP2D of rezatapopt when administered in combination with pembrolizumab. Secondary objectives of Phase 1b Combination Therapy are to characterize PK, safety and tolerability, and to assess preliminary efficacy of rezatapopt when administered in combination with pembrolizumab, including ORR. Enrollment into Phase 1b Combination Therapy is complete.
How this trial compares with your answers
Answer 2 more questions to improve match
What we know so far
Still need:
- • Tell us your age for better matching
- • Tell us your sex for better matching
Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.
Eligibility at a Glance
Key info
- Age: 12 Years and over
- Who can join: All genders
Biomarkers mentioned
Treatment history
Treatments you must have had:
- ✓ progressed on treatment
What the study is looking for
- ✓At least 18 years of age or 12 to 17 years of age after Safety Review Committee approval.
- ✓that has grown locally or that has spread solid cancer with a TP53 Y220C mutation
- ✓activity scale (ECOG) status of 0 or 1
- ✓Previously treated with one or more lines of anticancer therapy and progressive disease
- ✓healthy organ
Who cannot take part
- ✗Anti-cancer therapy within 21 days (or 5 half-lives) of receiving the the study treatment
- ✗Radiotherapy within 14 days of receiving the the study treatment
- ✗Primary CNS tumor
- ✗History of leptomeningeal disease or spinal cord compression
- ✗Brain metastases, unless neurologically stable and do not require steroids to treat associated neurological symptoms
See the full criteria
Where Is This Study? (2 UK sites)
Sarah Cannon Research Institute UK
London, United Kingdom
Freeman Hospital
Newcastle upon Tyne, United Kingdom
How to Get in Touch
PMV Pharma Clinical Study Information Center
Sponsor contactCONTACT
