Daruka Mahadevan, MD, PhD
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About Me
About Daruka Mahadevan, MD, PhD
Daruka Mahadevan, MD, PhD, is a professor of medicine at The University of Texas Health Science Center at San Antonio. He serves as co-chair and director of research at the UT Health San Antonio Multispecialty and Research Hospital. He is an internationally recognized physician-scientist in hematology and medical oncology.
Mahadevan earned a Bachelor of Science in physiology and biochemistry from the University of Reading in England and a doctorate in protein crystallography from the University of London. He received his Bachelor of Medicine and Bachelor of Surgery (MD equivalent) from King’s College Hospital Medical School at the University of London. He completed his residency in internal medicine at the University of Connecticut Health Center and a hematology-oncology fellowship at the University of Arizona Health Sciences Center. He is board-certified by the American Board of Internal Medicine and the American Board of Medical Oncology.
His major areas of interest include early-phase treatments for pancreatic cancer, gastrointestinal stromal tumors, myelodysplastic syndromes and non-Hodgkin lymphoma, including chronic lymphocytic leukemia. He has led or co-led early-phase clinical trials investigating new cancer agents, with funding from several National Institutes of Health grants and cancer research foundations. He also directed a drug discovery laboratory program based on his expertise in protein crystallography, leading to six U.S. patents for drugs targeting novel driver oncogenes—new cancer mutations that initiate or sustain cancer growth.
One of the drugs he developed, amuvatinib, targets c-Kit/c-Met/PDGFR/RAD51 and has advanced through Phase I and II clinical trials. As principal investigator or co-principal investigator on several NIH and foundation grants, he has established proof-of-concept in drug discovery (R01 AKT PH domain inhibitors) and drug development (NSF prostate cancer translational drug development, SPORE in lymphoma for Aurora kinase inhibitor therapy, and SWOG Hope Foundation targeted therapeutics for aggressive B- and T-cell non-Hodgkin lymphoma).
He has participated in multiple National Cancer Institute (NCI) advisory and leadership meetings, including external advisory board sessions and scientific leadership committee meetings. He received an NCI P30 supplement (2017–2019) to study rare cancers through whole-exome sequencing of tumor and normal samples in collaboration with the University of Arizona Genomics Core. From 2016 to 2019, he served as director of the Early Phase Therapeutics Program (“Phase I Program”), enrolling more than 150 patients in first-in-human investigational agent studies for both solid and hematologic malignancies.
Mahadevan continues to expand the early-phase therapeutics portfolio and investigator-initiated studies at UT Health San Antonio.
Gender
- Male
Languages Spoken
- English
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Credentials
Credentials
Positions
- Professor of Medicine, University of Texas Health Science Center San Antonio
- Chief, Division of Hematology-Medical Oncology, University of Texas Health Science Center San Antonio
- Director, Institute for Drug Development, UT Health San Antonio MD Anderson Cancer Center
- Associate Director, Clinical Research, UT Health San Antonio MD Anderson Cancer Center
Certifications
- American Board of Internal Medicine, Medical Oncology
Education
Medical School: King's College Hospital Medical School, University of London, England, UK
Fellowship: Hematology/Oncology, University of Arizona College of Medicine, Tucson, AZ
Residency: Internal Medicine, University of Connecticut School of Medicine, Farmington, CT
Doctorate: Protein crystallography, Birkbeck College, University of London, England, UK
Fellowship: Research, National Institute of Health, Bethesda, MD - Locations & Contact
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Research & Publications
Research & Publications
A comparative analysis of tumors and plasma circulating tumor DNA in 145 advanced cancer patients annotated by 3 core cellular processes
Larson K, Kannaiyan R, Pandey R, Chen Y, Babiker HM, Mahadevan D.
Cancers (Basel). 2020 Mar 16;12(3):701. doi: 10.3390/cancers12030701. PMID: 32188081; PMCID: PMC7140098.
View All Research & Publications
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Clinical Trials
Clinical Trials
Type of Cancer
Carcinoma
ClinicalTrials.gov Identifier
ClinicalTrials.gov registration not required
A Phase 1 Open-Label Study to Evaluate the Efficacy and Safety of ABBV-400 in Select Advanced Solid Tumor Indications
Type of Cancer
Chronic Lymphoid Leukemia, Lymphoma
ClinicalTrials.gov Identifier
NCT05512390
Principal Investigator
Daruka Mahadevan, MD, PhD
A First-In-Human Multicenter, Open-Label Study to Determine the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of ABBV-319 in B-cell Malignancies
M22-716 is a Phase 1, FIH, open-label, dose escalation, dose expansion, biomarker/pharmacodynamic (PD) study of ABBV-319 in participants with relapsed or refractory (R/R) B-cell malignancies.
Type of Cancer
Solid Tumor
ClinicalTrials.gov Identifier
ClinicalTrials.gov registration not required
Principal Investigator
Daruka Mahadevan, MD, PhD
A Phase 1/2 Dose Escalation and Cohort Expansion Study of LP-184 in Patients with Advanced or Metastatic Solid Tumors
To evaluate the safety, tolerability, MTD and the RP2D of LP-184 in patients with advanced solid tumors who have relapsed from or are refractory to standard therapy or for whom no standard therapy is available.
Type of Cancer
Solid Tumor, Metastases
ClinicalTrials.gov Identifier
NCT06244771
Principal Investigator
Daruka Mahadevan, MD, PhD
An Open-Label, Phase 1/2 Dose Escalation, Dose Expansion and Cohort Expansion Study Evaluating the Safety, PK and Clinical Activity of FMC-376 in Participants with KRAS G12C Mutated Locally Advanced Unresectable or Metastatic Solid Tumors (PROSPER)
This is an open-label, Phase 1/2, dose escalation, dose expansion and cohort expansion study to evaluate the safety, tolerability, PK, PD and clinical activity of FMC-376 in participants with locally advanced unresectable or metastatic solid tumors which harbor KRAS G12C mutation.
ClinicalTrials.gov Identifier
ClinicalTrials.gov registration not required
Principal Investigator
Daruka Mahadevan, MD, PhD
A PHASE 1, OPEN-LABEL, DOSE ESCALATION AND DOSE EXPANSION STUDY FOR LNCB74, A B7-H4 TARGETED ANTIBODY DRUG CONJUGATE, AS MONOTHERAPY IN PARTICIPANTS WITH ADVANCED SOLID TUMORS
The first-in-human clinical study will be a Phase 1, multicenter, open-label, multiple dose, two-part study of LNCB74 that will include Dose Escalation (Part 1) and Dose Expansion/Optimization (Part 2). The objectives of this study will be to determine the safety and tolerability, define the maximum tolerated dose (MTD), maximal administered dose (MAD) and/or the recommended Phase 2 dose (RP2D),…
Type of Cancer
Solid Tumor
ClinicalTrials.gov Identifier
NCT06792552
Principal Investigator
Daruka Mahadevan, MD, PhD
A Phase I First-in-human, Open-label, Multicenter Study to Investigate the Safety, Tolerability, Pharmacokinetics and Preliminary Antitumor Activity of SIM0505 in Adult Participants with Advanced Solid Tumors
Part 1 (dose escalation): to evaluate the safety and tolerability of SIM0505 and determine the maximum tolerated dose (MTD)