Unter wesntlicher Beteiligung von Evotec:
Forge Therapeutics Wins Powered by CARB-X Research Award of $8.8M to Accelerate Development of its LpxC Antibiotic to Kill the World’s Deadliest ‘Superbugs’ -Award recognizes Forge’s novel chemistry, novel class & novel MOA and highlights urgent need for new antibiotics- -Non-dilutive funding supports Forge’s efficient development strategy-
By Zak March 30, 2017 Press Releases
San Diego, Calif., March 30, 2017 – Forge Therapeutics, Inc., (“Forge”), a biotechnology company discovering first-in-class antibiotics using a breakthrough drug discovery platform, announced today a significant collaboration with CARB-X, (Combating Antibiotic Resistant Bacteria Accelerator), the world’s largest public-private partnership focused on funding the advancement of Gram-negative antibiotics. CARB-X selected Forge from a group of 168 international companies and research groups to be one of the first recipients of this novel cost-sharing award. Forge will receive an initial award of $4.8M over 15 months and potentially up to $4M from CARB-X after that period upon achievement of certain milestones.
CARB-X is supported by its partners around the globe including BARDA, NIH, Wellcome Trust, AMRC UK, California Life Science Institute, RTI, Mass Biotech Council, and Boston University. The CARB-X goal is to move promising antibacterial candidates, like Forge’s LpxC program, through the critical early stages of product development.
“The need for new antibiotics to solve the drug resistance epidemic is beyond urgent – resistant bacteria are clearly plentiful, but unfortunately, novel drugs are extremely rare. In partnership with Evotec, whose participation was key to our CARB-X application, we are tackling this global health issue from all sides – government, industry, charities – with the shared goal of reducing the worldwide death toll from ‘superbug’ bacterial infections,” said Zachary A. Zimmerman, Ph.D., CEO of Forge. “Because of this, we at Forge feel a tremendous sense of responsibility to advance our LpxC antibiotic program into the clinic as quickly as possible and we are thankful to CARB-X for their support of our efforts. In the next few years, we expect to advance the program to IND/Phase 1, which could yield the first novel Gram-negative antibiotic in decades.”
“Forge’s LpxC-inhibitor is an extremely important program to us,” said Dr. Mario Polywka, COO, Evotec AG, Forge’s strategic alliance partner. “The fact that CARB-X selected Forge as one of its first partners aligns with our assessment of the company’s innovative technology and capabilities to advance this program into the clinic and provide a much-needed new option against multi-drug resistant bacteria.”
In August 2016, CARB-X was launched to accelerate pre-clinical product development in the area of antibiotic-resistant infections, one of the world’s greatest health threats. CARB-X was established by BARDA and NIAID of the U.S. Department of Health and Human Services along with Wellcome Trust, a global charitable foundation dedicated to improving health. This partnership has committed up to $450 million in new funds over the next five years to increase the number of antibacterial products in the drug-development pipeline. It reflects a new approach to how antibacterial research and drug development is identified, funded and accelerated to the clinic.
About LpxC and the ‘Superbug’ Epidemic
Millions of people around the globe have become infected with bacteria that are resisted to current antibiotic treatments, or ‘superbugs’, creating a global health epidemic. An estimated 700,000 worldwide deaths occur each year from these drug-resistant infections, and in the U.S. alone, an estimated 23,000 people die each year from antibiotic resistant infections. The biotechnology industry, leading government agencies and world leaders agree that the need for new antibiotics is urgent.
LpxC is an attractive and highly sought after antibiotic target – it is conserved across Gram-negative bacteria and not found in Gram-positive bacteria or human cells. Other LpxC inhibitors have been evaluated by biopharma in the past but chemistry limitations (e.g. hydroxamic acid) have yielded ineffective compounds that suffer from poor drug-like properties. Thus, there are no approved therapeutics targeting LpxC. Forge, using its proprietary chemistry platform, has developed novel non-hydroxamate inhibitors of LpxC that are safe and effective in an animal model of Gram-negative infection and are able to kill Gram-negative ‘superbugs’ where other antibiotics are ineffective.
About Forge Therapeutics
Forge Therapeutics (“Forge”) is a privately-held biopharmaceutical company developing novel antibiotics to treat multi-drug resistant bacteria, or ‘superbugs’, that have ignited a global health epidemic. With its proprietary chemistry approach, Forge develops small molecule inhibitors targeting metalloenzymes. Forge’s lead effort is focused on LpxC, a zinc metalloenzyme found only in Gram-negative bacteria and which is essential for bacteria to grow. Forge has discovered novel small molecule inhibitors of LpxC that are potent in vitro, efficacious in vivo, and effective against drug resistant Gram-negative bacteria ‘superbugs’. To complement its innovative approach to drug discovery, Forge has an efficient business model that utilizes a mix of non-dilutive and traditional funding sources to advance its programs, including LpxC. Due to its expertise in the field, Forge has formed a strategic alliance with leading drug discovery alliance and development partnership company Evotec AG [Xetra:EVT] and has been awarded multiple government awards to address the global ‘superbug’ epidemic. In addition, Forge has amassed a rich intellectual property estate on metalloprotein inhibitors to protect its technology and pipeline. Forge maintains its headquarters in San Diego, California. To learn more please visit www.ForgeTherapeutics.com and follow us on Twitter @ForgeThera.
About CARB-X
CARB-X is the world’s largest public-private partnership devoted to antibacterial preclinical R&D. Funded by BARDA and Wellcome Trust, with in-kind support from NIAID, we will spend $450 million from 2017-2021 to support innovative products moving towards human clinical trials. CARB-X focuses on high priority drug-resistant bacteria, especially Gram-negatives. CARB-X is a charitable global public-private partnership led by Boston University School of Law. Other partners include the Broad Institute of Harvard and MIT, MassBio, the California Life Sciences Institute and RTI International. For more information, please visit www.carb-x.org and follow us on Twitter @CARB_X.
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