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NCT04246489 · ClinicalTrials.gov registry record · Phase 2

Bintrafusp Alfa Monotherapy in Platinum-Experienced Cervical Cancer

A Phase 2 study, sponsored by EMD Serono Research & Development Institute.

Completed
Registry status
Phase 2
Development phase
146
Enrollment target

NCT04246489: Completed Phase 2 study, sponsored by EMD Serono Research & Development Institute.

NCT04246489 is a Phase 2 study that has completed, run by EMD Serono Research & Development Institute. The registered enrollment target is 146 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (10% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04246489, a Phase 2 study, has completed, sponsored by EMD Serono Research & Development Institute.

COMPLETED
Registry status
Phase 2
Development phase
146 participants
Enrollment target

Study Summary

The main purpose of this study was to evaluate clinical efficacy and safety of bintrafusp alfa in participants with advanced, unresectable cervical cancer with disease progression during or after platinum-containing chemotherapy.

Primary Outcome

Confirmed objective response was defined as the number of participants with a confirmed objective response of complete response (CR) or partial response (PR). CR: Disappearance of all evidence of target and non-target lesions. PR: At least 30% reduction from baseline in the sum of the longest diameter (SLD) of all lesions. Confirmed CR = at least 2 determinations of CR at least 4 weeks apart and before progression. Confirmed PR = at least 2 determinations of PR at least 4 weeks apart and before

Interventions

  • DRUG Bintrafusp alfa

Trial Details

FieldValue
Enrollment Target 146 participants
Start Date 2020-03-30
Est. Completion 2022-12-14
Phase Phase 2

What the finished NCT04246489 record still lists

NCT04246489 is an interventional study that assigns participants to a tested intervention. The registered 146 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 (10% higher).

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

NCT04246489 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04246489 about?

NCT04246489 is a clinical study titled "Bintrafusp Alfa Monotherapy in Platinum-Experienced Cervical Cancer". The main purpose of this study was to evaluate clinical efficacy and safety of bintrafusp alfa in participants with advanced, unresectable cervical cancer with disease progression during or after platinum-containing chemotherapy.

What is the current status of trial NCT04246489?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 146 participants. The study started on 2020-03-30. Estimated completion is 2022-12-14.

What interventions are being tested in trial NCT04246489?

The interventions under investigation include: Bintrafusp alfa (DRUG).

Who is sponsoring clinical trial NCT04246489?

This trial is sponsored by EMD Serono Research & Development Institute, which has 81 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04246489's enrollment target sits among peer trials

146 496th of 2000 higher than 1,503 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 NCT04246489, the US trial registry maintained by the National Library of Medicine. NCT04246489 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.