drugset / Trial / NCT02584478

Phase 1/2a/3 Evaluation of Adding AL3818 to Standard Platinum-Based Chemotherapy in Subjects With Recurrent or Metastatic Endometrial, Ovarian, Fallopian, Primary Peritoneal or Cervical Carcinoma (AL3818-US-002)

NCT02584478

Phase 3 Unknown 294 enrolled Advenchen Laboratories, LLC
RandomizedParallel-groupOpen-labelTreatment

Summary

This trial is a Phase 1b/2a/3 trial designed to evaluate the safety and efficacy of adding oral AL3818 (Anlotinib, INN: Catequentinib), a Dual Receptor Tyrosine Kinase Inhibitor, to standard platinum-based chemotherapy concurrently in Subjects with Recurrent or Metastatic Endometrial, Ovarian, Fallopian, Primary Peritoneal or Cervical Carcinoma.

Timeline

Start
2015-12
Primary completion
2024-10
Completion
2024-12

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Catequentinib Small molecule 8 mg Oral
Subject Catequentinib Small molecule 12 mg Oral
Background Carboplatin Small molecule Intravenous
Background Doxorubicin Other / unclassified 40 mg/m2 Intravenous
Background Paclitaxel Small molecule 80 mg/m2 Intravenous
Background Paclitaxel Small molecule 175 mg/m2 Intravenous
Background Topotecan Small molecule 1.25 mg/m2 Intravenous
Background Topotecan Small molecule 4 mg/m2 Intravenous