Actively Recruiting

Age: 18Years - 75Years
All Genders
NCT06031636

Oncolytic Adenovirus(H101) Combined With PD-1 Inhibitors in Patients With Advanced Malignant Pleural Mesothelioma

Led by Tianjin Medical University Second Hospital · Updated on 2023-09-11

15

Participants Needed

1

Research Sites

158 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this study is to evaluate the efficacy and safety of Oncolytic Adenovirus(H101) combined with PD-1 inhibitor in patients with advanced malignant pleural mesothelioma who have previously been resistant to advanced PD-1 inhibitors.

CONDITIONS

Official Title

Oncolytic Adenovirus(H101) Combined With PD-1 Inhibitors in Patients With Advanced Malignant Pleural Mesothelioma

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18-75 years old (including boundaries), any gender
  • Confirmed late stage malignant pleural mesothelioma patients who have failed immunotherapy
  • Ability to understand and sign informed consent form by patient or legal representative
  • At least one lesion suitable for safe intratumoral or intrapleural injection, with diameter ≥ 1cm by spiral CT or ≥ 2cm by ordinary CT, measurable by imaging
  • ECOG performance status score between 0 and 2
Not Eligible

You will not qualify if you...

  • Physician believes patient cannot provide continuous follow-up information
  • Presence of any uncontrollable clinical problems such as severe mental, neurological, cardiovascular, respiratory, or other systemic diseases
  • Contraindications to oncolytic adenoviruses, PD-1 inhibitors, or related drugs

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Tianjin Medical Unversity Second Hospital

Tianjin, Tianjin Municipality, China

Actively Recruiting

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Research Team

H

Haitao Wang, Ph.D

CONTACT

J

Jinhuan Wang, Ph.D

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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