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NCT05446870 · ClinicalTrials.gov registry record · Phase 2

Pembrolizumab With Chemotherapy and MK-4830 for Treating Participants With Ovarian Cancer (MK-4830-002)

A Phase 2 study, sponsored by Merck Sharp & Dohme.

Completed
Registry status
Phase 2
Development phase
160
Enrollment target

NCT05446870: Completed Phase 2 study, sponsored by Merck Sharp & Dohme.

NCT05446870 is a Phase 2 study that has completed, run by Merck Sharp & Dohme. The registered enrollment target is 160 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (20% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05446870, a Phase 2 study, has completed, sponsored by Merck Sharp & Dohme.

COMPLETED
Registry status
Phase 2
Development phase
160 participants
Enrollment target

Study Summary

The primary objective is to evaluate in participants with high-grade serous ovarian cancer (HGSOC), whether the reduction from baseline in circulating tumor deoxyribonucleic acid (ctDNA) at Cycle 3 (ΔctDNA) is larger in participants receiving MK-4830 + pembrolizumab in combination with standard of care (SOC) therapy than in those receiving pembrolizumab + SOC therapy.

Primary Outcome

Blood samples were collected to determine levels of ctDNA. The fold change in the mean mutant/tumor molecules per mL (MTM/mL) at Cycle 3 from baseline is presented.

Interventions

  • BIOLOGICAL Pembrolizumab
  • DRUG Carboplatin
  • DRUG Paclitaxel
  • BIOLOGICAL MK-4830
  • BIOLOGICAL Avastin

Trial Details

FieldValue
Enrollment Target 160 participants
Start Date 2022-07-25
Est. Completion 2024-10-16
Phase Phase 2
Merck Sharp & Dohme

558 total trials

What the finished NCT05446870 record still lists

NCT05446870 is an interventional study that assigns participants to a tested intervention. The registered 160 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (20% higher).

The record links to 0 conditions, and to 5 interventions - of which Pembrolizumab is the first listed.

NCT05446870 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05446870 about?

NCT05446870 is a clinical study titled "Pembrolizumab With Chemotherapy and MK-4830 for Treating Participants With Ovarian Cancer (MK-4830-002)". The primary objective is to evaluate in participants with high-grade serous ovarian cancer (HGSOC), whether the reduction from baseline in circulating tumor deoxyribonucleic acid (ctDNA) at Cycle 3 (ΔctDNA) is larger in participants receiving MK-4830 + pembrolizumab in combination with standard of c...

What is the current status of trial NCT05446870?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 160 participants. The study started on 2022-07-25. Estimated completion is 2024-10-16.

What interventions are being tested in trial NCT05446870?

The interventions under investigation include: Pembrolizumab (BIOLOGICAL), Carboplatin (DRUG), Paclitaxel (DRUG), MK-4830 (BIOLOGICAL), Avastin (BIOLOGICAL).

Who is sponsoring clinical trial NCT05446870?

This trial is sponsored by Merck Sharp & Dohme, which has 558 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05446870's enrollment target sits among peer trials

160 422nd of 2000 higher than 1,559 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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

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Source: ClinicalTrials.gov NCT05446870, the US trial registry maintained by the National Library of Medicine. NCT05446870 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.