Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT04774952 · ClinicalTrials.gov registry record · Phase 1

Dose Escalation of RMC-5552 Monotherapy in Relapsed/Refractory Solid Tumors

A Phase 1 study, sponsored by Revolution Medicines.

Completed
Registry status
Phase 1
Development phase
58
Enrollment target

NCT04774952: Completed Phase 1 study, sponsored by Revolution Medicines.

NCT04774952 is a Phase 1 study that has completed, run by Revolution Medicines. The registered enrollment target is 58 participants, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04774952, a Phase 1 study, has completed, sponsored by Revolution Medicines.

COMPLETED
Registry status
Phase 1
Development phase
58 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the safety, tolerability, pharmacokinetic (PK), and pharmacodynamic (PD) profiles of escalating doses of RMC-5552 monotherapy in adult participants with relapsed/refractory solid tumors and to identify the recommended Phase 2 dose (RP2D).

Primary Outcome

Incidence, nature, and severity of treatment-emergent AEs and serious AEs, including incidence and severity of findings in laboratory values or vital signs for RMC-5552 monotherapy

Interventions

  • DRUG RMC-5552

Trial Details

FieldValue
Enrollment Target 58 participants
Start Date 2021-04-07
Est. Completion 2024-06-28
Phase Phase 1
Revolution Medicines

16 total trials

What the finished NCT04774952 record still lists

NCT04774952 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 58 participants, a relatively small participant target, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target.

The record links to 0 conditions, and to 1 intervention - of which RMC-5552 is the first listed.

NCT04774952 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04774952 about?

NCT04774952 is a clinical study titled "Dose Escalation of RMC-5552 Monotherapy in Relapsed/Refractory Solid Tumors". The purpose of this study is to evaluate the safety, tolerability, pharmacokinetic (PK), and pharmacodynamic (PD) profiles of escalating doses of RMC-5552 monotherapy in adult participants with relapsed/refractory solid tumors and to identify the recommended Phase 2 dose (RP2D).

What is the current status of trial NCT04774952?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 58 participants. The study started on 2021-04-07. Estimated completion is 2024-06-28.

What interventions are being tested in trial NCT04774952?

The interventions under investigation include: RMC-5552 (DRUG).

Who is sponsoring clinical trial NCT04774952?

This trial is sponsored by Revolution Medicines, which has 16 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04774952's enrollment target sits among peer trials

58 895th of 2000 higher than 1,100 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03587844 · 58 participants · Phase 2

    Dosing of Brentuximab Vedotin for Mycosis Fungoides, Sezary Syndrome Patients

  • NCT03630991 · 58 participants · Phase 1

    Edetate Calcium Disodium or Succimer in Treating Patients With Acute Myeloid Leukemia or Myelodysplastic Syndrome Undergoing Chemotherapy

  • NCT03949855 · 58 participants · Phase 2

    Belimumab With Rituximab for Primary Membranous Nephropathy

  • NCT04069273 · 58 participants · Phase 2

    Novel SEQUEnced Immunotherapy With Anti-angiogenesis and Chemotherapy in Advanced gastroesophageaL Adenocarcinoma

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT04774952, the US trial registry maintained by the National Library of Medicine. NCT04774952 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.