A Trial of SHR-A2102 With Adebrelimab With or Without Other Antitumor Therapy in Advanced or Metastatic Esophageal Cancer

Trial statusRecruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age18-70
SponsorShanghai Hengrui Pharmaceutical Co., Ltd.

About this trial

The study is being conducted to evaluate the safety, tolerability and efficacy of SHR-A2102 with Adebrelimab with or without other Antitumor Therapy in Advanced or Metastatic Esophageal Cancer. To explore the reasonable dosage of SHR-A2102 for Advanced or Metastatic Esophageal Cancer

Eligibility criteria

Qualifiers

Have the ability to give informed consent, have signed informed and able to comply with the treatment plan to visit the tests and other procedural requirements;

The age of signing the informed consent is 18 -70 years, regardless of gender;

Provide archived or fresh tumor tissue for vendor test;

At least one measurable lesion according to RECIST v1.1 criteria;

Disqualifiers

Inadequately treated central nervous system metastases or the presence of uncontrolled or symptomatic active central nervous system metastases;

Patients with uncontrolled tumor-related pain as determined by the investigator.

Moderate or severe ascites with clinical symptoms (i.e., those who required therapeutic puncture or drainage within 2 weeks before the study treatment, and only those who showed a small amount of ascites without clinical symptoms could be included in the study); Unable to control or moderate or higher amounts of pleural effusion or pericardial effusion

A history of gastrointestinal perforation and/or fistula within 6 months prior to initial medication, or significant tumor invasion of adjacent organs (large arteries or trachea, etc.), resulting in a higher risk of bleeding or fistula

Trial design

Treatments tested in this trial

  • SHR-A2102;Adebrelimab;Cisplatin

Treatment groups

148 Participants
are divided into 1 treatment group