Oak Hill Bio Launches With Pipeline and Senior Leadership From Takeda
Oak Hill Bio, a clinical-stage therapeutics company, has launched to develop medicines for extremely preterm infants and rare autoimmune diseases. The company has acquired a pipeline of six investigational therapeutics from Takeda Pharmaceutical, including two clinical-stage and four preclinical-stage programs. The lead candidate, OHB-607, aims to improve outcomes in premature infants and has shown promising Phase 2 results. Oak Hill plans to advance its clinical studies in 2022 and includes experienced executives from Takeda to support its mission.
- Acquisition of six investigational programs from Takeda enhances pipeline diversity.
- Lead candidate OHB-607 shows promising Phase 2 data for premature infants.
- Experienced executives from Takeda join the Oak Hill team for continuity.
- Significant unmet medical need addressed in premature infants and rare autoimmune diseases.
- None.
New Company Committed to Developing Life-Changing Medicines for Extremely Preterm Infants and Patients Suffering from Rare Autoimmune Diseases
Pipeline Includes Two Programs with Phase 2 Proof-of-Concept Data in Rare Diseases with Significant Unmet Need
Under the terms of the agreements, Takeda will receive an upfront payment, an ownership stake in Oak Hill and potential milestones and royalty payments in exchange for the acquired and licensed programs. Takeda will also support the transition for continued research and development of the acquired programs. The pipeline includes two clinical-stage and four preclinical-stage programs.
Two Takeda executives with direct experience working on the acquired programs will join Oak Hill, including
“Oak Hill has a significant opportunity to take these promising programs and advance them through clinical development to bring life-altering new medicines to patients in need,” said
Oak Hill’s lead therapeutic candidate, OHB-607 (formerly TAK-607), is a proprietary, recombinant version of insulin-like growth factor 1 (IGF-1), the natural version of which is a key driver of fetal growth and development in utero, and its binding protein, IGFBP-3.
Mothers are the primary source of IGF-1 for the developing fetus, with the fetus producing very little of its own until reaching 30 weeks of gestational age. At birth, extremely premature infants, born at less than 28 weeks of gestational age, have low levels of IGF-1 which are associated with greater complication rates. OHB-607, as a human IGF-1 replacement, is designed to help promote continued development and maturation of vital organs and the vasculature that supports them.
OHB-607 has been evaluated in both preclinical and clinical studies. A Phase 2 clinical trial showed a statistically significant shift towards milder bronchopulmonary dysplasia and a positive trend in reducing intraventricular hemorrhage (pre-specified secondary endpoints), with no significant safety signal observed.
“Every year, hundreds of thousands of infants worldwide are born extremely prematurely and, as a result, suffer from severe complications in their lungs, brain, and eyes that hinder their long-term development and quality of life. While prenatal steroids, surfactants, ventilators and improved resuscitation protocols have increased the survival rate of premature infants, there has been little progress in protecting their not fully developed organs from the trauma of life-saving measures at birth, including supplemental oxygen and breathing machines,” said
OHB-101 (Formerly TAK-752), a Phase 2a program, is currently being investigated for the treatment of a wide array of rare autoimmune diseases. It is a soluble recombinant version of the FcγR2B receptor that is designed to bind to immune complexes to prevent them from interacting with the fc gamma receptors that drive inflammation and autoimmune cascades. Preliminary clinical studies have been conducted in multiple autoimmune indications, including systemic lupus erythematosus, a rare autoimmune primary glomerular disease, and immune thrombocytopenia, a rare autoimmune blood disorder.
Oak Hill intends to advance the ongoing Phase 2b clinical study of OHB-607 for complications of premature birth in 2022 and initiate two Phase 2b clinical studies of OHB-101 in rare autoimmune diseases. The company also anticipates commencing IND-enabling activities for certain of its four preclinical programs, which include three novel anti-FCγR2B receptor monoclonal antibodies for autoimmune disease and an oral pKAL inhibitor for diabetic macular edema.
“There is a tremendous need for new therapies to prevent the complications of prematurity and for those suffering from rare autoimmune disorders,” said
Executive Team
Oak Hill’s executive team includes experienced biopharma executives, biotech entrepreneurs and financial operations and capital markets experts as well as rare disease and neonatology experts from Takeda:
-
Josh Distler , J.D., President and Chief Financial Officer, has extensive experience building and investing in biotechnology companies, having served as Head of Crossover and Quantitative Equity atAthanor Capital , COO of Global Private Investing forD. E. Shaw & Co. , Chief Operating Officer at Attenuon, a cancer drug development firm and as a Director of Schrödinger, Inc. -
Mark McHale , Ph.D., Chief Scientific Officer, most recently helped foundAslan Pharmaceuticals and served as its Chief Development Officer and Head of R&D. He has also held leadership positions with AstraZeneca and SmithKline Beecham (now GlaxoSmithKline Plc.). -
Victoria Niklas , M.D., Chief Medical Officer, has served in several roles at Takeda, including Global Program Leader of the OHB-607 program. She has extensive experience as a translational scientist and academic neonatologist including serving as Chief of theDivision of Neonatology for Nemours Children’s Hospital and Professor of Pediatrics, Division Chief and Medical Director, at UCLA’sOlive View Medical Center .
About Oak
Oak
View source version on businesswire.com: https://www.businesswire.com/news/home/20220201005520/en/
Investors
Oak
josh.distler@oakhillbio.com
Stern Investor Relations
Annemarie.fields@sternir.com
212-362-1200
Media
Ten
chris@tenbridgecommunications.com
617-834-0936
Source: Oak
FAQ
What is Oak Hill Bio's focus?
What are the main candidates in Oak Hill's pipeline?
What were the results of OHB-607's clinical trials?
When does Oak Hill plan to advance its clinical studies?