Clinical Focus

  • Medical Oncology

Academic Appointments

Professional Education

  • Board Certification: American Board of Internal Medicine, Medical Oncology (2024)
  • Fellowship: Dana Farber Cancer Institute Hematology Oncology Fellowship (2013) MA
  • Residency: Brigham and Women's Hospital Internal Medicine Residency (2010) MA
  • Medical Education: Harvard Medical School (2007) MA

Contact

  • Academic
    lgoyal@stanford.edu
    University - Faculty Department: Medicine - Med/Oncology Position: Associate Professor
  • Clinical (Primary)  Stanford Cancer Center 875 Blake Wilbur Dr Clinic A MC 6560 Stanford, CA 94305 (650) 498-6000 (fax)

Additional Clinical Info

Clinical Trials

  • AZD0901 in Participants With Advanced Solid Tumours Expressing Claudin18.2 Recruiting

    The purpose of this study is to assess the safety, tolerability, efficacy, pharmacokinetics (PK), and immunogenicity of AZD0901 as monotherapy and in combination with anti-cancer agents in participants with locally advanced unresectable or metastatic solid tumours expressing CLDN18.2.

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  • Study of Tinengotinib VS. Physician's Choice a Treatment of Subjects With FGFR-altered in Cholangiocarcinoma Recruiting

    This study is a Phase III, Randomized, Controlled, Global Multicenter Study to Evaluate the Efficacy and Safety of Oral Tinengotinib versus Physician's Choice in Subjects with Fibroblast Growth Factor Receptor (FGFR)-altered, Chemotherapy- and FGFR Inhibitor-Refractory/Relapsed Cholangiocarcinoma

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  • A Study of an FGFR2/3 Inhibitor (CGT4859) in Patients With Cholangiocarcinoma and Other Advanced Solid Tumors Not Recruiting

    This is an open-label, phase 1/2 study evaluating the safety, tolerability, pharmacokinetic (what the body does to the drug), pharmacodynamic (what the drug does to the body), and antitumor activity of CGT4859 in adult participants with intrahepatic cholangiocarcinoma (iCCA) or other advanced solid tumors with FGFR2 and/or FGFR3 genetic alternations.

    Stanford is currently not accepting patients for this trial.

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  • Rilvegostomig + Chemotherapy as Adjuvant Therapy for Biliary Tract Cancer After Resection (ARTEMIDE-Biliary01) Not Recruiting

    A global study to assess the efficacy and tolerability of rilvegostomig compared to placebo in combination with investigator's choice of chemotherapy in participants with BTC after surgical resection with curative intent.

    Stanford is currently not accepting patients for this trial.

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  • Study of XL092 in Combination With Immuno-Oncology Agents in Subjects With Solid Tumors Not Recruiting

    This is a multicenter Phase 1b, open label, dose-escalation and cohort-expansion study, evaluating the safety, tolerability, PK, preliminary antitumor activity, and effect of biomarkers of XL092 administered alone, and in combination with nivolumab (doublet), nivolumab + ipilimumab (triplet) and nivolumab + relatlimab (triplet) in subjects with advanced solid tumors. In the Expansion Stage, the safety and efficacy of XL092 as monotherapy and in combination therapy will be further evaluated in tumor-specific Expansion Cohorts.

    Stanford is currently not accepting patients for this trial.

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2025-26 Courses