Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This combination chemotherapy regimen, frequently referred to as TAD-HAM, is a sequential induction therapy used for the treatment of adult patients with newly diagnosed acute myeloid leukemia (AML). It was developed and extensively evaluated by the German AML Cooperative Group (AMLCG), with Prof. Dr. Wolfgang Hiddemann serving as a primary investigator. The regimen consists of two sequential courses: TAD (thioguanine, cytarabine, and daunorubicin) followed by HAM (high-dose cytarabine and mitoxantrone). The components work synergistically to eliminate leukemic blasts; cytarabine and thioguanine are antimetabolites that interfere with DNA synthesis and repair by inhibiting DNA polymerase and incorporating into nucleic acids, while daunorubicin and mitoxantrone are DNA-intercalating agents that inhibit topoisomerase II, leading to double-strand breaks and apoptosis.
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 cytarabine + mitoxantrone + daunorubicin + thioguanine.