Cristal Therapeutics, a clinical-stage pharmaceutical company developing targeted nanomedicines for the treatment of cancer and other diseases with high unmet patient need, today announced three upcoming poster presentations that highlight CPC634 positive data from its three phase 1 safety and biodistribution studies at the ASCO 2019 meeting, Chicago, Illinois May 31st - June 4th.

CPC634 is Cristal Therapeutics’ lead nanomedicine candidate. It is a new drug modality that entraps the clinically validated chemotherapy docetaxel as its therapeutic payload with CriPec® nanoparticles.

Axel Mescheder, M.D., CEO/CMO, Cristal Therapeutics said, "We are excited to present data from our ongoing CPC634 clinical development program at ASCO. The results presented are from the first human trials that utilize Cristal Therapeutics’ CriPec® nanoparticle technology. CPC634 was specifically designed to overcome the toxic systemic side effects associated with current docetaxel products by enabling enhanced accumulation and ensure sustained release at the tumor site to optimize the therapeutic/safety balance.
Convincing safety, pharmacokinetic and biodistribution data from our first-in-human studies further strengthen our approach to clinically develop CPC634 as the superior nanomedicine alternative to Taxotere®, a conventional docetaxel product."

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