Doxorubicin is under clinical development by InnoMedica and currently in Phase II for Solid Tumor. According to GlobalData, Phase II drugs for Solid Tumor have a 10% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Doxorubicin’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.

GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.

Doxorubicin overview

Doxorubicin (TLD-1, Talidox) is under development for the treatment of advanced solid tumors such as ovarian cancer and breast cancer as a third line therapy. The drug candidate is administered intravenously as a liposomal formulation. It is developed based on liposomal targeting technology. The technology involves encapsulation of the drug candidate in a liposome with sugar chain, sialyl Lewis X attached to the liposome surface for targeting.

InnoMedica overview

InnoMedica discovers and develops therapeutics for the treatment of cancer. The company develops drugs using its proprietary drug delivery technology, Talidox, based on the transport and release of active pharmaceutical agents, locally, at the target area. Its pipeline portfolio includes targeted liposomal doxorubicin TLD-1/Talidox for the treatment of advanced metastatic tumors. The company’s pipeline portfolio also includes other candidates for the therapeutic areas of autoimmune diseases such as multiple sclerosis, arteriosclerosis and chronic inflammatory diseases. It operates through a office and production facility in Bern and Marly located in Switzerland, respectively. InnoMedica is headquartered in Zug, Switzerland.

For a complete picture of Doxorubicin’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 2 September 2023

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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.

GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.