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    Richard Law

    Senior Equity Research Analyst at Goldman Sachs

    Richard Law is a Senior Equity Research Analyst at Goldman Sachs, specializing in SMID-cap biotechnology companies. He provides research coverage on major biotech firms within the small and mid-cap space, consistently achieving a 45.16% success rate with an average return of 5.86% on his stock recommendations according to third-party analyst ratings platforms. Richard Law began his career in equity research and has established himself at Goldman Sachs, leveraging deep sector expertise and analytical rigor, and holds professional credentials and regulatory approvals for equity research and trading. Recognized for his contributions, Law continually delivers actionable investment insights grounded in both quantitative metrics and industry trends.

    Richard Law's questions to Mineralys Therapeutics (MLYS) leadership

    Richard Law's questions to Mineralys Therapeutics (MLYS) leadership • Q2 2025

    Question

    Richard Law from Goldman Sachs asked about lorunderstat's potential in combination with drugs other than SGLT2s, scenarios where competitor data could impact partnership talks, and whether partners view ASIs as similar or seek a best-in-class drug.

    Answer

    CEO Jon Congleton highlighted that aldosterone drives comorbidities like CKD and OSA, suggesting broad potential beyond SGLT2 combinations. He noted that while fixed-dose combinations are contemplated, U.S. physicians often prefer separate agents for dosing flexibility. He reiterated confidence in lorunderstat's value, stating the market has room for two ASIs and that lorunderstat has a distinct profile, but declined to speculate on partner perspectives.

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    Richard Law's questions to Crinetics Pharmaceuticals (CRNX) leadership

    Richard Law's questions to Crinetics Pharmaceuticals (CRNX) leadership • Q2 2025

    Question

    Richard Law of Goldman Sachs questioned how much can be learned from the 10-patient Cohort 4 in the CAH study, given potential data variability, and asked if there's a chance to adjust the Phase III protocol based on these findings since the Phase III is starting before the Cohort 4 data is available.

    Answer

    Chief Medical & Development Officer Dana Pizzuti acknowledged that Cohort 4 is assessing AM vs. PM dosing but stated the Phase III protocol is already "locked and loaded" for PM dosing. She confirmed that sites are already starting up for the Phase III trial and the company does not plan to make any changes to the protocol based on the Cohort 4 results.

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    Richard Law's questions to Arcutis Biotherapeutics (ARQT) leadership

    Richard Law's questions to Arcutis Biotherapeutics (ARQT) leadership • Q2 2025

    Question

    Richard Law of Goldman Sachs asked about Zareve's classification in Medicare negotiations (i.e., within the topical steroid class or a separate PDE4 class), the progress made in securing Medicaid access over the last quarter, and if there was any new thinking on the ex-US commercial opportunity.

    Answer

    Chief Commercial Officer Todd Edwards clarified that Zareve is positioned within the broad dermatology topical basket for Medicare, which is considered advantageous. He highlighted exceptional progress in Medicaid, with over half of recipients now having access. President and CEO Frank Watanabe affirmed that the company's stance on ex-US opportunities has not changed, citing the challenging reimbursement landscape in Europe as a key factor.

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