Ixazomib domestic generic · multiple myeloma Bioequivalence Study

According to official protocol filings (target population synthesized by CMDN from study details, not an official CDE field), this study is primarily designed for patients with [Multiple myeloma]. Eligibility requires verified clinical confirmation by investigators regarding prior lines of therapy, active disease biomarkers, and performance status.

According to verified protocol filings, key eligibility thresholds include: age 18–75 years, ECOG performance status ≤ 1. The study specifies 7 inclusion and 24 exclusion criteria covering detailed organ function and medical history. Final enrollment confirmation is determined by investigators at participating hospital trial centers.

The core therapeutic target or investigational mechanism is [Ixazomib domestic generic]. It aims to selectively eradicate clonal plasma cells or redirect anti-tumor immune responses, representing an active area of precision hematology research.

This study is registered as a [Bioequivalence Study] clinical trial. The protocol is conducted under rigorous ethical and Good Clinical Practice (GCP) oversight approved by institutional ethics committees.

This is an international multi-centre study with 0 study centres in China and 2 overseas centres. The lead institution is [The First Affiliated Hospital of Henan University of Science and Technology]. Prominent sites include The First Affiliated Hospital of Henan University of Science and Technology, Changzhou No. 1 People's Hospital. Eligible domestic patients can seek screening at the nearest participating centre.

The official public registration identifier for this protocol is [CTR20253002] (CDE_CTR). Patients and researchers can verify registration details and regulatory authorizations directly on the official NMPA CDE platform.