Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
EIA is a combination chemotherapy regimen consisting of etoposide, ifosfamide, and doxorubicin (adriamycin), developed by Heidelberg University for the treatment of high-risk soft tissue sarcoma. The regimen is typically administered in a neoadjuvant and adjuvant setting alongside surgery and radiotherapy, as investigated in the Phase II NeoWTS trial (NCT01382030). Its mechanism of action involves the synergistic effects of three cytotoxic agents: ifosfamide, an alkylating agent that cross-links DNA; doxorubicin, an anthracycline that intercalates into DNA and inhibits topoisomerase II; and etoposide, a podophyllotoxin derivative that also targets topoisomerase II to induce double-stranded DNA breaks. This intensive protocol is designed to provide both local and systemic control for patients with high-risk features such as large tumor size and high histological grade.
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 etoposide + ifosfamide + doxorubicin.