Signs 2nd Clinical Trial Collaboration and Supply Agreement
Genome and Co., a leading global microbiome anti-cancer drug development company, signed a second clinical trial collaboration and supply agreement (CTCSA) with Merck KGaA of Germany and Pfizer Inc. with the aim of developing the world’s first immuno-oncology microbiome therapeutic.
The collaboration follows the first agreement with Merck and Pfizer in December 2019 to conduct the first combination clinical trial of avelumab (BAVENCIO®) and GEN-001 (NCT04601402, “Study 101”).
The objective of the clinical trial (“Study 201”) under this newly entered CTCSA is to investigate the efficacy and safety of the combination of GEN-001 and avelumab for gastric and gastroesophageal junction adenocarcinoma that continue to be difficult to treat. This trial will be conducted simultaneously at six or more hospital and medical center sites in the Republic of Korea.
With this clinical trial, Genome and Co. will proceed with Phase 2a to assess the efficacy and safety of the combination of GEN-001 and avelumab using the defined recommended phase 2 dose (RP2D) of GEN-001 in combination with avelumab. Merck and Pfizer will supply avelumab for use in the new company-led clinical trial, Study 201. The extended clinical collaboration between Genome and Co. and Merck and Pfizer marks the first time that two consecutive clinical development collaborations have been executed between combination partnersfor immuno-oncology microbiome treatment.
Genome and Company is developing GEN-001 through an efficient clinical development roadmap in cooperation with experts in the field. The company is leading clinical trials in systematic approaches to immediately advance to phase 2 upon the completion of a phase 1 study. Also, the company has achieved IND clearance by the US FDA and MFDS of the Republic of Korea for a variety of patient demographics as well as cancer types.
Genome and Co. CEO Pae Ji-soo said, “This second CTCSA with Merck and Pfizer is the achievement of our outstanding R&D capabilities and the effective clinical collaboration that is established through the ongoing Study 101. We would be able to reach the oncology leadership position using immuno-oncology microbiome treatment, especially in the Asian market, through the additional clinical trial.”
Under the terms of these agreements, Genome and Co. will be the sponsor of the studies, and Merck and Pfizer will supply avelumab for both Study 101 and Study 201. Both parties will have access to the clinical data.