Bora Han
Vice President, Preclinical Development @ Attovia Therapeutics
About
* Accomplished biopharmaceutical leader with 20 years experience in drug development, inclusive of nonclinical safety/toxicology, DMPK, pharmacology, regulatory affairs, and drug development operations * Expertise in multiple biopharmaceutical drug modalities: small molecues, monoclonal antibody, peptibody, fusion protein, bi-specific antibody, antibody drug conjugates (ADC), antibody oligo nucleotide conjugates, CAR-T, antibody-conjugated cellular therapy, and oligonucleotides. * In depth experience in oncology and immuno-oncology * In depth experience in therepeutic areas requiring special delivery route (i.e. ophthamology, inhaled respiratory therapy, and intra-articular administration for osteoarthritis) * Successfully created and headed nonclinical development function in start up and mid-size public biotech companies managing safety, DMPK, regulatory, and pharmacology * Held positions as a therapeutic area lead and functional area lead for a global large pharmaceutical company * Successfully led nonclinical development from concept to registration in multiple therapeutic areas and modalities—oncology, inflammation, ophthalmology, cardiovascular disorder, neurosciences, metabolic disorder, and pain * Successfully managed industry and academic collaborations * Served as the nonclinical expert in business development activities for in-licensing, out-licensing, and fund raising * Expertise in global regulatory strategy (nonclinical) with authoring and filing of numerous IND, NDA, and BLA * Portfolio leadership role for a prolific research unit within big biopharmaceutical company managing multiple high level scientists
United States
San Francisco Bay Area
Biotechnology
Drug Discovery, IND, Biomarkers, Drug Development, Biopharmaceuticals, Translational Medicine, Inflammation, Monoclonal Antibodies, Drug Metabolism, Clinical Development, Toxicology, Pharmacodynamics, GLP, Biologics, NDA, Pharmacokinetics, Translational Research, Pharmacology, Biotechnology, In Vivo
Experience

Vice President, Preclinical Safety
South San Francisco
• Responsible for nonclinical development and safety strategy including toxicology, pathology, pharmacokinetics, bioanalytics, and regulatory submission. • Additional duties include planning and execution of clinical biomarker strategy and translational oncology • Successfully planned and executed nonclinical strategy for accelerated clearance of IND for entry into the clinic in crowded and competitive space

Vice President, Preclinical Development
Adheren Inc.
Emeryville
Bora Han's Contact Information
Phone
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