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NCT07525791 · ClinicalTrials.gov registry record · Phase 1

A Research Study Looking Into How NNC0662-0419 Works With Birth Control Pills and Emptying of the Stomach in Women Not Able to Become Pregnant With Excess Body Weight

A Phase 1 study, sponsored by Novo Nordisk A/S.

Recruiting
Registry status
Phase 1
Development phase
45
Enrollment target

NCT07525791: Recruiting Phase 1 study, sponsored by Novo Nordisk A/S.

NCT07525791 is a Phase 1 study that is actively recruiting participants, run by Novo Nordisk A/S. The registered enrollment target is 45 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (25% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07525791, a Phase 1 study, is actively recruiting participants, sponsored by Novo Nordisk A/S.

RECRUITING
Registry status
Phase 1
Development phase
45 participants
Enrollment target

Study Summary

The purpose of this clinical study is to find out if NNC0662-0419 is safe and effective to be taken together with other medicines, like birth control pills, and emptying of the stomach in women not able to become pregnant living with overweight or obesity. There are 3 study treatments in this study, participants will get all of the treatments, NNC0662-0419 the treatment being tested, Altavera a type of birth control pill, Acetaminophen a common type of mild painkiller.

Primary Outcome

Measured as picograms per milliliter (h\*pg/mL)

Interventions

  • DRUG Acetaminophen
  • DRUG NNC0662-0419
  • DRUG Oral contraceptive

Trial Details

FieldValue
Enrollment Target 45 participants
Start Date 2026-04-07
Est. Completion 2027-05-04
Phase Phase 1
Novo Nordisk A/S

431 total trials

What NCT07525791 shows while recruiting

NCT07525791 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 45 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (25% lower).

The record links to 0 conditions, and to 3 interventions - of which Acetaminophen is the first listed.

NCT07525791 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07525791 about?

NCT07525791 is a clinical study titled "A Research Study Looking Into How NNC0662-0419 Works With Birth Control Pills and Emptying of the Stomach in Women Not Able to Become Pregnant With Excess Body Weight". The purpose of this clinical study is to find out if NNC0662-0419 is safe and effective to be taken together with other medicines, like birth control pills, and emptying of the stomach in women not able to become pregnant living with overweight or obesity. There are 3 study treatments in this study,...

What is the current status of trial NCT07525791?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 45 participants. The study started on 2026-04-07. Estimated completion is 2027-05-04.

What interventions are being tested in trial NCT07525791?

The interventions under investigation include: Acetaminophen (DRUG), NNC0662-0419 (DRUG), Oral contraceptive (DRUG).

Who is sponsoring clinical trial NCT07525791?

This trial is sponsored by Novo Nordisk A/S, which has 431 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07525791's enrollment target sits among peer trials

45 1066th of 2000 higher than 915 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 NCT07525791, the US trial registry maintained by the National Library of Medicine. NCT07525791 (small enrollment · none site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.