Johnson is a veteran biopharmaceutical and healthcare leader with more than 25 years of experience in developing drugs and growing companies.
Johnson is currently the chief executive officer at VelosBio, a clinical-stage oncology company developing novel antibody-drug-conjugates and bispecific antibodies.
Prior to VelosBio, he was CEO at Acerta Pharma, an oncology-focused pharmaceutical company, where he led the company through a critical phase of growth from approximately 40 to over 150 employees and from a signal-seeking first-in-human trial to more than 20 active clinical studies.
Under his leadership, the company designed and launched three registration-directed trials, including two global Phase 3 trials for acalabrutinib, an irreversible oral Bruton's tyrosine kinase inhibitor initially focused on hematological malignancies.
Johnson's time at Acerta culminated in the execution of a strategic transaction with AstraZeneca valued at up to USD 7bn.
He has raised over USD 500m in biopharma-directed capital and has extensive experience in deal making.
David's prior experience spans from pre-clinical development to all phases of clinical development through product launch. He has made significant contributions to drugs ultimately garnering regulatory approvals, including bortezomib (Velcade), romidepsin (Istodax), idelalisib (Zydelig), and acalabrutinib (Calquence).
Before his time as CEO at Acerta Pharma and his founding of VelosBio, David held roles with increasing responsibilities within commercial, pipeline development, medical affairs, and clinical development organizations at companies including Hoffman-La Roche, Immunex (acquired by Amgen), Millennium (acquired by Takeda), Favrille, Gloucester (acquired by Celgene), and Calistoga (acquired by Gilead).
He is a co-author on numerous publications, including three New England Journal of Medicine articles, and holds a bachelor's degree from Indiana University.
Zentalis Pharmaceuticals is a clinical-stage biopharmaceutical company focused on developing clinically differentiated, novel small molecule therapeutics that target fundamental biological pathways in cancer.
In addition to its lead program, ZN-c5, an oral selective estrogen receptor degrader for estrogen-receptor-positive, HER2-negative breast cancer, the company is developing a broad pipeline of oncology candidates, targeting areas of major unmet medical need.
The company has offices in New York and San Diego.
Charles River Laboratories launches AMAP to reduce animal testing reliance
PureTech completes enrollment in Phase 2b ELEVATE IPF trial for LYT-100
Cybin secures additional US patent for CYB003 breakthrough therapy programme
GSK's meningitis vaccine candidate accepted for FDA review
Innovent Biologics names new Oncology CMO
UroGen's UGN-103 IND accepted by FDA for bladder cancer treatment
Biophytis reinforces obesity IP with new patent application
MaaT Pharma reveals positive 18-month data for MaaT013 in GI-aGvHD
Fusion Antibodies plc secures contract for OptiPhage library development
Innate Pharma advances Sanofi-developed NK cell engager to Phase 2 for blood cancer patients
AbbVie announces interim evaluation of Atogepant Phase three, open-label 156-week extension study