Clinical Study on the Efficacy and Safety of Iparomlimab and Tuvonralimab Injection Combined With Nab-Paclitaxel in Neoadjuvant Therapy for Locally Advanced Resectable Esophageal Squamous Cell Carcinoma

ConditionESCC
Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorTianjin Medical University Cancer Institute and Hospital

About this trial

Major objectives to evaluate the efficacy and safety of Iparomlimab and Tuvonralimab Injection (QL1706,an Anti-PD-1/CTLA-4 Combined Antibody) combined with Nab-Paclitaxel in neoadjuvant therapy for patients with locally advanced resectable esophageal squamous cell carcinoma.

Eligibility criteria

Qualifiers

Voluntarily understand and sign the informed consent form for this study.

Age ≥ 18 years, male or female.

Histologically or cytologically confirmed thoracic ESCC (Stage T1-2N1-2M0 or T3N0-2M0, according to the AJCC 8th edition).

ECOG performance status of 0-2.

Disqualifiers

Inability to comply with the study protocol or study procedures.

Presence of supraclavicular lymph node metastasis.

Obvious tumor invasion of organs adjacent to the esophageal lesion.

Evidence of esophagomediastinal or tracheoesophageal fistula found on imaging within 4 weeks before enrollment.

Trial design

Treatments tested in this trial

  • lparomlimab and Tuvonralimab Injection in Combination with Nab-Paclitaxel

Treatment groups

26 Participants
are divided into 1 treatment group

Locations

1
Tianjin Medical University Cancer Institute and Hospital300000, TianjinTianjin Municipality, China

Sponsors and collaborators

Tianjin Medical University Cancer Institute and Hospital

Lead sponsor