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NCT04907968 · ClinicalTrials.gov registry record · Phase 1

Study of Upifitamab Rilsodotin in Combination With Carboplatin in Participants With High-grade Serous Ovarian Cancer

A Phase 1 study, sponsored by Mersana Therapeutics.

Terminated
Registry status
Phase 1
Development phase
31
Enrollment target

NCT04907968: Clinical Trial Phase 1 study, sponsored by Mersana Therapeutics.

NCT04907968 is a Phase 1 study that was terminated before completion, run by Mersana Therapeutics. The registered enrollment target is 31 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (48% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04907968, a Phase 1 study, was terminated before completion, sponsored by Mersana Therapeutics.

TERMINATED
Registry status
Phase 1
Development phase
31 participants
Enrollment target

Study Summary

Phase 1 safety study of the antibody-drug conjugate (ADC) XMT-1536 (upifitamab rilsodotin) administered as an intravenous infusion once every four weeks in combination with Carboplatin in participants with high-grade serous ovarian cancer (HGSOC, including fallopian tube and primary peritoneal cancer). The trial consists of dose escalation (DES) and expansion (EXP) portion. In addition to safety assessments, the pharmacokinetics of the drug will be assessed along with ADC activity.

Primary Outcome

Determine the MTD of Upifitamab rilsodotin in combination with carboplatin by evaluating adverse events in combination with carboplatin

Interventions

  • DRUG Carboplatin
  • DRUG XMT-1536 (Upifitamab Rilsodotin)

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2021-06-11
Est. Completion 2023-10-03
Phase Phase 1
Mersana Therapeutics

11 total trials

Why NCT04907968 stopped before completion

NCT04907968 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 31 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (48% lower).

The record links to 0 conditions, and to 2 interventions - of which Carboplatin is the first listed.

NCT04907968 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04907968 about?

NCT04907968 is a clinical study titled "Study of Upifitamab Rilsodotin in Combination With Carboplatin in Participants With High-grade Serous Ovarian Cancer". Phase 1 safety study of the antibody-drug conjugate (ADC) XMT-1536 (upifitamab rilsodotin) administered as an intravenous infusion once every four weeks in combination with Carboplatin in participants with high-grade serous ovarian cancer (HGSOC, including fallopian tube and primary peritoneal cance...

What is the current status of trial NCT04907968?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 31 participants. The study started on 2021-06-11. Estimated completion is 2023-10-03.

What interventions are being tested in trial NCT04907968?

The interventions under investigation include: Carboplatin (DRUG), XMT-1536 (Upifitamab Rilsodotin) (DRUG).

Who is sponsoring clinical trial NCT04907968?

This trial is sponsored by Mersana Therapeutics, which has 11 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04907968's enrollment target sits among peer trials

31 1322nd of 2000 higher than 669 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

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Source: ClinicalTrials.gov NCT04907968, the US trial registry maintained by the National Library of Medicine. NCT04907968 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.