Tarian Pharma continues to advance its clinical pipeline with strong momentum: Our third clinical trial has been submitted to European Medicines Agency (EMA). This is TARIAN-008 for the prevention of Hand-Foot Syndrome associated with capecitabine treatment of breast and colorectal cancer. The 24-subject study is planned to initiate in early Q12026, targeting a high-need toxicity area with limited preventive options.
TARIAN-014 – Chemotherapy-Induced Peripheral Neuropathy (CIPN) associated with taxane treatment of breast cancer. The 30-subject trial is actively enrolling. CIPN remains a major driver of dose reductions and treatment discontinuation.
TARIAN-007 – EGFR-inhibitor–induced folliculitis (colorectal cancer): The 60-subject trial continues to progress, with 15 patients enrolled to date. EGFRi-related cutaneous reactions are among the most common and treatment-disruptive toxicities in oncology.
Together, these programs strengthen the clinical foundation for TAR-0520, our topical gel designed to prevent and mitigate chemotherapy- and targeted-therapy–related skin toxicities which are a huge burden for cancer patients.
Indeed , 80% of cancer patients suffer cutaneous toxicities leading to:





At Tarian Pharma, we stand at the intersection of science and empathy — committed to protecting patients, supporting clinicians, and shaping a future where cancer care is not only effective, but profoundly human.
Our solution isn’t just patient-friendly — it’s also designed for seamless integration into oncology protocols.
Simple and compatible, it helps clinicians focus on what matters most: remission, recovery, and results. It improves compliance, reduces interruptions, and supports overall treatment success.
At Tarian Pharma, our purpose focuses on one concrete solution: Tarian Gel, our oncogical support shield. Engineered with science, designed with empathy, and built to preserve treatment continuity — it represents everything we stand for.
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