Ze Tian

Head of Pharmacology and Translation

Brookline, Massachusetts, United States

About

• A highly motivated, interactive, creative PhD scientist with 20+ years’ experience in cancer drug discovery • Experience in leading research teams to advance preclinical drug development programs from target identification and validation, through IND enabling • Facilitate earlier clinical programs with biomarker validation, dose -schedule justification, and rational combination strategies • Strong expertise in PK/PD/efficacy relationship and experience in syngeneic, xenograft, humanized and GEMM models

Experience

  • Head of pharmacology and Translational Science, Group Leader at Oncology Research for Biologics and Immunotherapy Translation (ORBIT), MD Anderson
    Oct 2015 - Present · 10 yrs 9 mos

    Manage a team of pharmacologists; lead strategic planning, execution and reporting of pre-clinical pharmacology and toxicology studies; provide oversight, scientific guidance and mentorship to in vivo biologists to ensure high quality data across a range of projects and influence/impact projects broadly across the portfolio • in vivo/ex vivo target validation, PK/PD/efficacy and MoA for antibody and cell therapy • in vivo discovery of novel immune-oncology targets using shRNA and CRISPR technology • Established and characterized relevant syngeneic, GEMM, CDX, PDX and a variety of humanized models for internal programs • Non-GLP PK, Tox/TK in rodent and NHP • IND enabling for the section of preclinical pharmacology; 8F4 antibody in phase I clinical trial • Manage CROs and academic collaboration • develop animal protocol, ensure good practice on animal welfare, vivarium regulation and IACUC protocol

  • ORBIT (Oncology Research for Biologics and Immunotherapy Translation) (8 yrs 6 mos)
    • Head of Non-clinical
      Jul 2021 - Mar 2024 · 2 yrs 9 mos

      Drove strategic program initiation and portfolio enrichment for new therapeutic opportunities while providing functional leadership for the biology, pharmacology, PK/PD, safety, and translational sciences team. In this latter capacity, I ensured the delivery of high-quality, PCC/IND packages and provided scientific mentorship critical to advancing the broader portfolio.

    • Principal Research Scientist
      Jul 2019 - Jun 2021 · 2 yrs

    • Senior Research Scientist
      Feb 2017 - Jun 2019 · 2 yrs 5 mos

  • Staff Scientist, head of in vivo group at Curis.Inc.
    Jan 2014 - Sep 2015 · 1 yr 9 mos

    Led a group of scientists with research focusing on efficacy, combination strategy, PK/PD relationship, biomarker identification/validation and toxicity with small molecules in oncology and Immuno oncology to advance preclinical programs and facilitate earlier clinical programs • Developed and characterized a panel of syngeneic and xenograft models for ICB and targeted therapy • Investigated PK/PD/efficacy of the investigational drugs as a single agent or in combination • Drafted preclinical pharmacology and drug safety parts of IND filing fimepinostat, annual report, DSUR and IB; FDA granted fast track designation of R/R lymphoma. • Evaluated tolerability, toxicity and TK profile in rodent • Acted as an internal preclinical pharmacology and safety expertise during the due diligence process • Managed CROs and academic collaboration

  • Staff Scientist at Curis, Inc., Boston, MA
    Jan 2014 - Sep 2015 · 1 yr 9 mos

    Managed programs and led a team of scientists focusing on PK/PD/efficacy relationships, toxicity, clinical biomarker identification/validation and combination strategies of small molecules in oncology and immuno-oncology. Supported the progression of clinical programs and drove the advancement of preclinical programs.

  • Dana Farber Cancer Institute and Harvard Medical School (5 yrs 6 mos)
    • Instructor
      Jul 2010 - Jan 2014 · 3 yrs 7 mos

      Focused on anti-cancer drug discovery with specification in Multiple Myeloma (MM) in various cancer pathways; major research interests included target validation, signal transduction and biomarker identification as well as drug efficacy in distinct animal models • Elucidated MoA and efficacy of first in class USP7 inhibitor p5091, which provides the framework for targeting USP7 to develop the next generation UPS-based novel therapeutics. • Explored signaling pathways and efficacy of proteasome inhibitor MLN9708 (ixazomib), which was approved by FDA for MM. • Explored and determined the role of miRNA-33b as a tumor suppressor in MM upon MLN9708 treatment • Dissected the MoA and efficacy of b-AP15, which led to the first in class DUB inhibitor in clinical trial in MM.

    • Research Fellow
      Aug 2008 - Jun 2010 · 1 yr 11 mos