Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This is a combination therapy consisting of two agents: temozolomide, an oral alkylating agent, and trastuzumab emtansine (T-DM1), an antibody-drug conjugate. Temozolomide acts as a DNA-methylating agent that induces cytotoxicity in dividing tumor cells. Trastuzumab emtansine combines the HER2-targeting monoclonal antibody trastuzumab with the microtubule inhibitor DM1 via a stable linker, enabling targeted delivery of cytotoxic payload to HER2-overexpressing cancer cells. The combination has been investigated primarily for the prevention of additional brain metastases in patients with HER2-positive breast cancer who have already developed brain metastases and received local treatment. Phase 1 studies indicate this regimen is safe and well tolerated, with main toxicities being mild laboratory abnormalities such as thrombocytopenia and leukopenia[1][4][2].
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 temozolomide + trastuzumab emtansine.