TIMELINE
Actuate Therapeutics announces FDA acceptance of IND application for 9-ING-41 and clearance to proceed with clinical study in patients with advanced cancers Acutate Therapeutics submits IND application for treatment of refractory cancers. Actuate Therapeutics receives rare pediatric disease designation for 9-ING-41 for treatment of neuroblastoma. FDA grants an additional Orphan Drug Designation for 9-ING-41 for the treatment of neuroblastoma. Actuate closes Series A Financing totaling $3.8M Dr. Matsangou presents research on GSK-3B and its role in head and neck carcinoma at the AACR meeting in Washington, DC. Actuate technologies featured in the Molecular Pathways special feature section in the journal Clinical Cancer Research. Dr. Francis J. Giles joins Actuate as Chief Medical Officer. (press release) FDA grants 9-ING-41 an Orphan Drug Designation for treatment of glioblastoma. Actuate receives a favorable FDA Written Response to our Pre-IND Plan for the development of 9-ING-41. The FDA laid out a very clear path on tasks necessary to complete in order to submit an IND, which sets the company up well for advancing 9-ING-41 into the clinic, and ultimately, to effectively treating patients. Actuate completes initial financing. Andrey Ugolkov presents his work the use of 9-ING-41 in treatment-sensitive and treatment-resistant glioblastoma at the Society of Neuro Oncology meeting. (see attachment) Actuate Forms Scientific Advisory Board License agreements are executed with both UIC and Northwestern for the technology and know-how that serves as the foundational intellectual property for Actuate Therapeutics. Company is incorporated as Apotheca Therapeutics, Inc, a Delaware C Corp, with Headquarters in Fort Worth, Texas.
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