Cure8

Why This Matters

A new Phase 2 study is testing an investigational injectable drug (called “627”) for moderate to severe ulcerative colitis. People with UC who have not responded to or cannot tolerate current therapies are the intended population, so the trial could be relevant to those seeking new treatment options.

Who Should Pay Attention

Adults with moderate–severe UC, patients with inadequate response or intolerance to current UC therapies, clinicians treating UC, and researchers following drug development for IBD.

Study Snapshot

Story typeClinical Reference
Trial phasePhase 2
Enrollment288 participants
Study statusRecruiting
Source depthTrial registry record

What To Know

This is a Phase 2 interventional clinical trial (NCT07507513) testing an investigational injectable drug referred to as “627” versus placebo in adults with moderate to severe ulcerative colitis (UC). The study is recruiting and plans to enroll about 288 participants across multiple dose groups, with safety (adverse events) tracked through a 36‑week period.

The trial enrolls adults (18–75) with at least 3 months of UC and who have moderate–severe active disease and prior inadequate response, loss of response, intolerance to one or more therapies, or corticosteroid dependence. It uses subcutaneous injections of 627 at several dose levels and includes a placebo arm.

The record lists standard eligibility and exclusion criteria (e.g., infection screening, recent major surgery, malignancy history, vaccine restrictions, contraception requirements). Locations include a site in Guangzhou, China. This entry is a trial registry record describing planned study design and not trial results.

No efficacy or safety results are reported in this registry entry; it describes the study protocol, arms, and primary safety outcome (adverse events) only.

Keep In Mind

This is a clinicaltrials.gov registry record describing a planned Phase 2 trial (protocol-level information). The record does not include study results; it documents design, eligibility, interventions, and planned safety outcome. As with any registered trial, enrollment, conduct, and results may change over time.

Source Details

Review the original publication for the complete reporting, methods, and context.

Read Original Source
Clinical trial Evidence type derived from source or registry metadata.
PublicationClinicalTrials.gov
SponsorSunshine Guojian Pharmaceutical (Shanghai) Co., Ltd.
Trial IDNCT07507513
Study typeInterventional
Trial phasePhase 2
Enrollment288 participants
Indexed viaClinicalTrials.gov
Source typeTrial registry record
PublishedJul 28, 2026, 12:00 AM
Content availableTrial registry record

This Cure8 brief is based on source text from the linked article. Cure8 is informational only and is not a substitute for professional medical advice, diagnosis, or treatment.

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