Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The MATRix regimen is a high-dose chemoimmunotherapy protocol primarily utilized as the induction phase for fit patients with newly diagnosed primary central nervous system lymphoma (PCNSL). It consists of four agents: methotrexate (antimetabolite), cytarabine (antimetabolite), thiotepa (alkylating agent), and rituximab (anti-CD20 monoclonal antibody). The regimen was established following the IELSG32 randomized phase 2 trial, which demonstrated superior complete remission rates and survival outcomes compared to methotrexate-cytarabine combinations with or without rituximab. Its mechanism involves a multi-pronged attack on malignant B-cells: methotrexate and cytarabine inhibit DNA synthesis by interfering with folate metabolism and DNA polymerase activity, respectively; thiotepa causes DNA cross-linking through alkylation; and rituximab induces antibody-dependent cellular cytotoxicity and complement-mediated lysis of CD20-positive cells. This combination is designed to maximize blood-brain barrier penetration and systemic efficacy.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on MATRix.