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NCT07017699 · ClinicalTrials.gov registry record

A Study to Assess Deucravacitinib Safety in Pregnancy

A clinical trial of Psoriasis (PsO), sponsored by Bristol-Myers Squibb.

Recruiting
Registry status
900
Enrollment target
1
Study location

NCT07017699: Recruiting study of Psoriasis (PsO), sponsored by Bristol-Myers Squibb.

NCT07017699 is a study of Psoriasis (PsO) that is actively recruiting participants, run by Bristol-Myers Squibb. The registered enrollment target is 900 participants, below the 1,018-participant average among 3 other Psoriasis (PsO) trials with a reported enrollment target (12% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07017699, a study of Psoriasis (PsO), is actively recruiting participants, sponsored by Bristol-Myers Squibb.

RECRUITING
Registry status
900 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to assess pregnancy and infant outcomes among pregnant participants enrolled in an established North American pregnancy registry (Organization of Teratology Information Specialists \[OTIS\]) who were exposed to deucravacitinib.

Conditions Studied

Interventions

  • DRUG Deucravacitinib
  • DRUG Other systemic treatments for PsO

Study Locations (1)

California

  • University of California San Diego - La Jolla

Trial Details

FieldValue
Enrollment Target 900 participants
Start Date 2025-03-21
Est. Completion 2029-02-28
Bristol-Myers Squibb

1,025 total trials

What NCT07017699 shows while recruiting

NCT07017699 is an observational study that tracks outcomes without assigning an intervention. The registered 900 participants enrollment target is mid-sized for trials with a published cap, below the 1,018-participant average among 3 other Psoriasis (PsO) trials with a reported enrollment target (12% lower).

The record links to 1 condition, with Psoriasis (PsO) appearing as the primary indexed condition, and to 2 interventions - of which Deucravacitinib is the first listed.

NCT07017699 reports a single indexed study location in California.

Frequently Asked Questions

What is clinical trial NCT07017699 about?

NCT07017699 is a clinical study titled "A Study to Assess Deucravacitinib Safety in Pregnancy". The purpose of this study is to assess pregnancy and infant outcomes among pregnant participants enrolled in an established North American pregnancy registry (Organization of Teratology Information Specialists \[OTIS\]) who were exposed to deucravacitinib.

What is the current status of trial NCT07017699?

This trial is currently recruiting. The enrollment target is 900 participants. The study started on 2025-03-21. Estimated completion is 2029-02-28.

What conditions does trial NCT07017699 study?

This clinical trial studies the following conditions: Psoriasis (PsO).

What interventions are being tested in trial NCT07017699?

The interventions under investigation include: Deucravacitinib (DRUG), Other systemic treatments for PsO (DRUG).

Who is sponsoring clinical trial NCT07017699?

This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07017699 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT07017699, the US trial registry maintained by the National Library of Medicine. NCT07017699 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.