SAN DIEGO, CA, USA I March 31, 2014 I Sorrento Therapeutics, Inc. (NASDAQ: SRNE; Sorrento), a late-stage clinical oncology company developing new treatments for cancer and associated pain, today announced that the first patient has been dosed in the pivotal clinical trial designed to support approval of Cynviloq for the treatment of metastatic breast cancer and non-small cell lung cancer.
The registration trial referred to as TRIBECA™ (TRIal designed to evaluate BioEquivalence between Cynviloq™ and Abraxane®; clinicaltrials.gov identifier: NCT02064829) is an open-label, randomized, multi-center, single-dose, crossover registration study being conducted at clinical sites across the U.S., EU, and Singapore. A projected 100 patients with metastatic or locally recurrent breast cancer will be administered 260 mg/m2 of Cynviloq or 260 mg/m2 of Abraxane using a 30 minute infusion in a crossover design to compare the bioequivalence of both drugs. Based on the End-of-Phase II meeting with the U.S. Food and Drug Administration (FDA) in July 2013, this trial was designed to gain marketing approval for Cynviloq under the 505(b)(2) regulatory pathway in the U.S. Sorrento expects to file a New Drug Application with the FDA in the first half of 2015.
“The initiation of the TRIBECA trial represents a very important milestone in the development of Cynviloq as well as in the progression of our pipeline,” said Henry Ji, PhD, President and CEO of Sorrento.
“Cyniviloq has already demonstrated bioequivalence in our animal studies, and we believe it has commercially-beneficial administration and storage properties compared to Abraxane,” said Vuong Trieu, Ph.D., CSO of Sorrento and co-inventor of Abraxane. “We are particularly pleased with the response shown by investigators who have exhibited strong interest in participating in this clinical trial.”
Lee Schwartzberg MD, Medical Director of the West Clinic said, “As a breast cancer investigator, I am excited about participating in the TRIBECA trial. Patients are always in need of new options to treat their cancer, and Cyniviloq could be a very important addition to our treatment armamentarium.”
About Cynviloq™
Cynviloq (IG-001 or Genexol-PM®; a paclitaxel-loaded micellar diblock copolymer) is a next-generation branded paclitaxel formulation for the potential treatment of metastatic breast cancer, non-small cell lung cancer, pancreatic cancer, and other solid tumors. In July 2013, the FDA Division of Oncology Products 1 agreed that the 505(b)(2) BE approach is the appropriate regulatory pathway, using Abraxane® and Taxol® as the Reference Listed Drugs, to obtain approval. Sorrento initiated the single bioequivalence trial required for registration, on March 31, 2014.
Sorrento has exclusive distribution rights to Cynviloq™ in the U.S., the 27 countries of the European Union, Mexico, Canada, and Australia from Samyang Biopharmaceuticals, a South Korean corporation. Cynviloq is being marketed in Korea, Vietnam, Phillipines, India, and Thailand under the names of Paxus-PM® and Genexol-PM.
About Sorrento Therapeutics, Inc.
Sorrento is an oncology company developing new treatments for cancer and associated pain. Sorrento’s most advanced asset Cynviloq™, the next-generation paclitaxel, will commence its registrational trial and be developed under the abbreviated 505(b)(2) regulatory pathway. Sorrento is also developing RTX, a non-opiate TRPV1 agonist currently in a Phase 1/2 study at the National Institutes of Health to treat terminal cancer patients suffering from intractable pain. The Company has made significant advances in developing human monoclonal antibodies, complemented by a comprehensive and fully integrated Antibody Drug Conjugate (ADC) platform that includes proprietary conjugation chemistries, linkers, and toxic payloads. Sorrento’s strategy is to enable a multi-pronged approach to combating cancer with small molecules, therapeutic antibodies, and ADCs.
SOURCE: Sorrento Therapeutics
Post Views: 64
SAN DIEGO, CA, USA I March 31, 2014 I Sorrento Therapeutics, Inc. (NASDAQ: SRNE; Sorrento), a late-stage clinical oncology company developing new treatments for cancer and associated pain, today announced that the first patient has been dosed in the pivotal clinical trial designed to support approval of Cynviloq for the treatment of metastatic breast cancer and non-small cell lung cancer.
The registration trial referred to as TRIBECA™ (TRIal designed to evaluate BioEquivalence between Cynviloq™ and Abraxane®; clinicaltrials.gov identifier: NCT02064829) is an open-label, randomized, multi-center, single-dose, crossover registration study being conducted at clinical sites across the U.S., EU, and Singapore. A projected 100 patients with metastatic or locally recurrent breast cancer will be administered 260 mg/m2 of Cynviloq or 260 mg/m2 of Abraxane using a 30 minute infusion in a crossover design to compare the bioequivalence of both drugs. Based on the End-of-Phase II meeting with the U.S. Food and Drug Administration (FDA) in July 2013, this trial was designed to gain marketing approval for Cynviloq under the 505(b)(2) regulatory pathway in the U.S. Sorrento expects to file a New Drug Application with the FDA in the first half of 2015.
“The initiation of the TRIBECA trial represents a very important milestone in the development of Cynviloq as well as in the progression of our pipeline,” said Henry Ji, PhD, President and CEO of Sorrento.
“Cyniviloq has already demonstrated bioequivalence in our animal studies, and we believe it has commercially-beneficial administration and storage properties compared to Abraxane,” said Vuong Trieu, Ph.D., CSO of Sorrento and co-inventor of Abraxane. “We are particularly pleased with the response shown by investigators who have exhibited strong interest in participating in this clinical trial.”
Lee Schwartzberg MD, Medical Director of the West Clinic said, “As a breast cancer investigator, I am excited about participating in the TRIBECA trial. Patients are always in need of new options to treat their cancer, and Cyniviloq could be a very important addition to our treatment armamentarium.”
About Cynviloq™
Cynviloq (IG-001 or Genexol-PM®; a paclitaxel-loaded micellar diblock copolymer) is a next-generation branded paclitaxel formulation for the potential treatment of metastatic breast cancer, non-small cell lung cancer, pancreatic cancer, and other solid tumors. In July 2013, the FDA Division of Oncology Products 1 agreed that the 505(b)(2) BE approach is the appropriate regulatory pathway, using Abraxane® and Taxol® as the Reference Listed Drugs, to obtain approval. Sorrento initiated the single bioequivalence trial required for registration, on March 31, 2014.
Sorrento has exclusive distribution rights to Cynviloq™ in the U.S., the 27 countries of the European Union, Mexico, Canada, and Australia from Samyang Biopharmaceuticals, a South Korean corporation. Cynviloq is being marketed in Korea, Vietnam, Phillipines, India, and Thailand under the names of Paxus-PM® and Genexol-PM.
About Sorrento Therapeutics, Inc.
Sorrento is an oncology company developing new treatments for cancer and associated pain. Sorrento’s most advanced asset Cynviloq™, the next-generation paclitaxel, will commence its registrational trial and be developed under the abbreviated 505(b)(2) regulatory pathway. Sorrento is also developing RTX, a non-opiate TRPV1 agonist currently in a Phase 1/2 study at the National Institutes of Health to treat terminal cancer patients suffering from intractable pain. The Company has made significant advances in developing human monoclonal antibodies, complemented by a comprehensive and fully integrated Antibody Drug Conjugate (ADC) platform that includes proprietary conjugation chemistries, linkers, and toxic payloads. Sorrento’s strategy is to enable a multi-pronged approach to combating cancer with small molecules, therapeutic antibodies, and ADCs.
SOURCE: Sorrento Therapeutics
Post Views: 64
