Report workspace tools

NCT05688852TERMINATEDanonymous

A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of VTX958 in Participants With Moderately to Severely Active Crohn's Disease

Sponsor

Source record

Ventyx Biosciences, Inc

Phase

Source record

PHASE2

Modality

AI-normalized

small molecule

Target

AI-normalized

VTX958, VTX958, VTX958 Placebo

Indication / condition

AI-normalized

Crohn Disease

Intervention

Source record

VTX958, VTX958, VTX958 Placebo

Source & freshness

Source record

NCT ID

NCT05688852

Original source

ClinicalTrials.gov

Source last updated

Jul 03, 2025

Ingested at

Jun 11, 2026

Internal sync

Jun 11, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

Open original registry record
View original source fields

NCT ID

NCT05688852

Title

A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of VTX958 in Participants With Moderately to Severely Active Crohn's Disease

Sponsor

Ventyx Biosciences, Inc

Status

TERMINATED

Phase

PHASE2

Condition raw

Crohn Disease

Condition normalized

Crohn Disease

Modality raw

small molecule

Modality normalized

small molecule

Target raw

VTX958, VTX958, VTX958 Placebo

Target normalized

VTX958, VTX958, VTX958 Placebo

Interventions

VTX958, VTX958, VTX958 Placebo

Public preview

Source record

This is a multicenter, randomized, double-blind placebo-controlled, parallel group study to evaluate the efficacy and safety of VTX958 in participants with moderately to severely active Crohn's Disease.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

Report access

Create an account to unlock this report

Choose the access model that matches the job: one urgent report, reusable credits for project work, or unlimited monthly access with AI and folders.

Full protocol, outcomes, eligibility, contacts and results sections
Patent/IP landscape with verified records when available
Board-ready PDF export with source provenance
Save to folders and synthesize multiple assets in premium workspace
Create account

Create a free account first, then unlock a single report, buy credits or subscribe.