Actively Recruiting

Phase 2
Age: 18Years - 75Years
All Genders
NCT07102901

Safety and Efficacy of SHR2554 Combined With Other Antitumor Therapies in Gastric or Gastro-oesophageal Junction Adenocarcinoma

Led by Jiangsu HengRui Medicine Co., Ltd. · Updated on 2025-09-10

351

Participants Needed

2

Research Sites

116 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This is a multicenter, phase 2, open label study to evaluate safety, tolerability and efficacy of SHR2554 combined with other anti-tumor treatments in patients with advanced or metastatic gastric or gastroesophageal junction adenocarcinoma.

CONDITIONS

Official Title

Safety and Efficacy of SHR2554 Combined With Other Antitumor Therapies in Gastric or Gastro-oesophageal Junction Adenocarcinoma

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • At least 18 years old or the minimum legal adult age when signing consent
  • Has at least one measurable lesion by CT or MRI based on RECIST v1.1 at screening
  • Willing to provide an adequate tumor sample
  • Eastern Cooperative Oncology Group performance status (ECOG PS) of 0 or 1 at screening
Not Eligible

You will not qualify if you...

  • Difficulty swallowing or other issues preventing oral intake of SHR2554
  • Prior treatment with any enhancer of zeste homolog inhibitors
  • Uncontrolled or significant cardiovascular disease
  • Spinal cord compression or active central nervous system metastases requiring treatment
  • Active autoimmune diseases needing systemic corticosteroids or immunosuppressants
  • Known allergy to SHR2554 or its ingredients
  • Ongoing uncontrolled systemic infections needing intravenous antibiotics, antivirals, or antifungals
  • Diagnosis of other cancers within 5 years before starting study treatment
  • History or current interstitial lung disease, pneumonitis requiring steroids, or significant lung disease
  • Psychological, social, familial, or geographical factors preventing regular follow-up

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Harbin Medical University Cancer Hospital

Harbin, Heilongjiang, China, 150081

Actively Recruiting

2

The First Affiliated Hospital of Zhengzhou University

Zhengzhou, Henan, China, 450052

Actively Recruiting

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Research Team

B

Botao Zhu

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

4

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