Clarity Pharmaceuticals announces US FDA grants Cu-64 SARTATE™ Orphan Drug Designation for the clinical management of neuroblastoma

Sydney, Australia 19 May 2020 – Clarity Pharmaceuticals, a radiopharmaceutical company focused on the treatment of serious disease, is pleased to announce that the U.S. Food and Drug Administration (FDA) has granted Orphan Drug Designation (ODD) for 64Cu-SARTATE™ as a diagnostic agent for the clinical management of neuroblastoma. “This milestone comes shortly after the FDA…

Clarity Pharmaceuticals Announces US FDA Grants Cu-67 SARTATE™ Orphan Drug Designation for Neuroblastoma

Sydney, Australia 21 April 2020 – Clarity Pharmaceuticals, a radiopharmaceutical company focused on the treatment of serious disease, is pleased to announce that the U.S. Food and Drug Administration (FDA) has granted Orphan Drug Designation (ODD) for 67Cu-SARTATE™, a therapy for the clinical management of neuroblastoma. Neuroblastoma most often occurs in children younger than 5…

Prof. Oliver Sartor Joins Clarity’s Advisory Board

Sydney, Australia 19 March 2020 – Clarity Pharmaceuticals, a radiopharmaceutical company focused on the treatment of serious disease, is pleased to announce that Prof. Oliver Sartor has joined Clarity’s Advisory Board. Prof. Sartor is a medical oncologist and an internationally recognised expert in prostate cancer. He is the Laborde Professor for Cancer Research, Medical Director…

Clarity appoints Dr Gillies O’Bryan-Tear to Chair Newly Formed Global Clinical Development Group

Sydney, Australia 31 March 2020 – Clarity Pharmaceuticals, a radiopharmaceutical company focused on the treatment of serious disease, is pleased to announce that Dr Gillies O’Bryan-Tear will be chairing Clarity’s newly formed Global Clinical Development group. Dr O’Bryan-Tear joined the pharmaceutical industry in 1986 where he has spent 30 years in clinical development, medical management and…

Clarity Pharmaceuticals Signs Copper-67 Supply Agreement with Idaho State University’s Idaho Accelerator Center

Sydney, Australia 13 March 2020 – Clarity Pharmaceuticals, a radiopharmaceutical company focused on the treatment of serious disease, is pleased to announce the signing of a Product Supply Agreement with the Idaho State University Idaho Accelerator Center (IAC) for the production and commercial supply of copper-67 (Cu-67). Under the new agreement, IAC will supply Clarity…

NorthStar Medical Technologies Signs Letter of Intent with Clarity Pharmaceuticals to Supply Therapeutic Radioisotope Copper-67 (Cu-67)

BELOIT, Wis. and Sydney, Australia – February 11, 2020 – NorthStar Medical Technologies, LLC (NorthStar), a global innovator in the production and distribution of radioisotopes used for medical imaging, and Clarity Pharmaceuticals, a radiopharmaceutical company focused on the treatment of serious disease, today announced the signing of a Letter of Intent for the commercial supply…

Dr Colin Biggin Moves to Managing Director and CEO, Dr Matthew Harris Resigns from the Board

Sydney, Australia 30 October 2019 – Clarity Pharmaceuticals, a radiopharmaceutical company focused on the treatment of serious disease, is pleased to announce that interim-CEO, Dr Colin Biggin, has moved to Managing Director and CEO of the Company, to lead Clarity through the next stages of clinical development and commercialisation. Dr Biggin’s background in radiopharmaceutical development…

Dr Jennifer Rosenthal Appointed Director of Quality and Regulatory Affairs

Sydney, Australia 23 October 2019 – Clarity Pharmaceuticals, a radiopharmaceutical company focused on the treatment of serious disease, is pleased to announce the appointment of Dr Jennifer Rosenthal as Director of Quality and Regulatory Affairs. Jennifer has more than 20 years’ management experience in the biotechnology industry, serving in senior director and executive level roles…

Clarity Receives US FDA response on its Theranostic Investigational New Drug (IND) Application that the study may proceed

Sydney, Australia 3 October 2019 – Clarity Pharmaceuticals, a radiopharmaceutical company focused on the treatment of serious disease, is pleased to announce that it has received a response on its Investigational New Drug (IND) application that the study may proceed from the U.S. Food and Drug Administration (FDA) for a Phase 1-2a theranostic (i.e. diagnostic…