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  • Home
  • Company
    • Team
  • Technology
    • TARTIS rationale
    • TARTIS disease targets
  • Pipeline
    • OT-82
  • News

OncoTartis completed a non-GLP formal toxicology study of OT-82 on rats (21 day) and monkeys (28 days) and successfully determined a safe dose range for human clinical studies. These studies are planned to be repeated under GLP conditions starting in 1Q15.

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OncoTartis completed a non-GLP formal toxicology study of OT-82 on rats (21 day) and monkeys (28 days) and successfully determined a safe dose range for human clinical studies. These studies are planned to be repeated under GLP conditions starting in 1Q15.

I78-tfw_yef-dg_rt 2014-10-30T18:04:13+00:00 October 30th, 2014|

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Recent News

  • OncoTartis, Inc. and Children’s Cancer Institute announced the publication of two research manuscripts in a leading onco-hematological journal Leukemia, both devoted to the OncoTartis’ clinical drug candidate OT-82. January 16, 2020
  • First patient has been recruited and received his first OT-82 treatment! July 17, 2019
  • Oncotartis, Inc has received a green light from FDA for its IND application. The Company will start engaging clinical sites immediately. It plans to use 5-10 clinical sites to conduct the trial. February 27, 2019
  • OncoTartis, Inc has hired a global, full-service contract research organization (CRO), Clinipace, to conduct a Phase 1/2a trial of its drug candidate OT-82 acting against hematological cancers. December 3, 2018
  • OncoTartis, Inc. has engaged Dr. Eric Rowinsky to serve an acting Medical Director. March 14, 2018

Contact Info

640 Ellicott St, Suite 480 Buffalo, NY 14203

Phone: 716.858.3055

Email: [email protected]

Web: www.oncotartis.com

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