{"id":933568,"date":"2026-02-03T08:03:31","date_gmt":"2026-02-03T13:03:31","guid":{"rendered":"https:\/\/www.marketnewsdesk.com\/index.php\/spruce-biosciences-adds-regulatory-and-clinical-development-expertise-to-leadership-team\/"},"modified":"2026-02-03T08:03:31","modified_gmt":"2026-02-03T13:03:31","slug":"spruce-biosciences-adds-regulatory-and-clinical-development-expertise-to-leadership-team","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/spruce-biosciences-adds-regulatory-and-clinical-development-expertise-to-leadership-team\/","title":{"rendered":"Spruce Biosciences Adds Regulatory and Clinical Development Expertise to Leadership Team"},"content":{"rendered":"

<\/p>\n

Spruce Biosciences Adds Regulatory and Clinical Development Expertise to Leadership Team<\/b><\/p>\n

Daven Mody, Pharm.D., Appointed as Senior Vice President, Regulatory and Quality<\/i><\/p>\n

Bruno Gagnon, B.Pharm., M.Sc., Appointed as Senior Vice President, Clinical Development<\/i>Operations<\/i><\/p>\n

SOUTH SAN FRANCISCO, Calif.–(BUSINESS WIRE<\/a>)–Spruce Biosciences, Inc.<\/a> (Nasdaq: SPRB), a late-stage biopharmaceutical company focused on developing and commercializing novel therapies for neurological disorders with significant unmet medical need, today announced the appointments of Daven Mody, Pharm.D., as Senior Vice President of Regulatory and Quality and Bruno Gagnon, B.Pharm., M.Sc., as Senior Vice President, Clinical Development Operations.<\/p>\n

\n\u201cWe are delighted to welcome both Daven and Bruno to the executive leadership team during a transformative time for Spruce,\u201d said Javier Scwarzberg, M.D., M.P.H., Chief Executive Officer of Spruce Biosciences. \u201cDaven\u2019s regulatory expertise is unparalleled across the industry, and his significant experience from successful filings and approvals of multiple NDAs and MAAs will be instrumental as we prepare for the BLA submission and seek potential U.S. FDA approval of our tralesinidase alfa enzyme replacement therapy (TA-ERT) program for the treatment of Sanfillipo Syndrome Type B (MPS IIIB). I believe that Bruno\u2019s global leadership experience in rare disease drug development, including in MPS diseases, will drive the successful clinical execution of our planned confirmatory study of TA-ERT and other pipeline programs.\u201d<\/p>\n

\nDaven Mody, Pharm.D., brings over 25 years of regulatory affairs experience, guiding global development programs across multiple therapeutic areas including rare diseases. He most recently served as Senior Vice President, Regulatory Affairs and Quality at Lassen Therapeutics, Ocelot Bio, and Blade Therapeutics, working as team lead on investigational programs for multiple ophthalmologic, hepatic, pulmonary, hepatic, and oncology indications for which he helped secure several orphan drug and fast track designations. Earlier, he served as Head of Regulatory Affairs at Theravance Biopharma and Impax Laboratories where he led the efforts in the first-round approvals of YUPELRI\u00ae<\/sup> for COPD and RYTARY\u00ae <\/sup>for Parkinson\u2019s Disease, respectively, by both the U.S. FDA and EMA. Dr. Mody began his career at ALZA Corporation and since held roles of increasing leadership responsibility within regulatory affairs at Matrix Pharmaceuticals, Genentech, CoTherix, Johnson & Johnson, and Medivation. He also founded AZURA Life Sciences, LLC, a regulatory and quality consultancy. He received a Pharm.D. from the University of the Pacific and an MBA from California State University, East Bay. Dr. Mody is certified by the Regulatory Affairs Certification Board.<\/p>\n

\nBruno Gagnon, B.Pharm., M.Sc., joins Spruce Biosciences with more than 30 years of experience leading clinical operations for global drug development programs. As Senior Vice President of Global Clinical Operations at Opthea, Mr. Gagnon oversaw clinical program execution for a Phase 3 pivotal wet age-related macular degeneration (wet AMD) program and took on interim responsibility for medical affairs and pharmacovigilance. Previously, he led development operations for BridgeBio Pharma\u2019s affiliate, Eidos Therapeutics, where he oversaw strategic planning and operational execution of clinical trials for the company\u2019s TTR amyloidosis program and played a key role in advancing ATTRUBY\u00ae (Acoramidis) towards regulatory approval. Earlier, he served as Vice President of Clinical Operations at BioMarin, directing rare disease clinical programs and global trial execution for six compounds across all stages of development. He earned his M.Sc. in pharmaceutical sciences and drug development from the University of Montreal and a B.S. in pharmacy from Laval University.<\/p>\n

Inducement Awards<\/b><\/p>\n

\nIn connection with Dr. Mody\u2019s and Mr. Gagnon\u2019s employment with Spruce, on February 2, 2026 each of Dr. Mody and Mr. Gagnon were granted restricted stock units (RSUs) for 5,500 shares of Spruce\u2019s common stock. While the inducement awards are being made outside of Spruce\u2019s 2020 Equity Incentive Plan, the awards will be subject to terms and conditions generally consistent with those set forth under such plan and the award agreements thereunder. The Compensation Committee of the Board of Directors approved the awards as an inducement material to Dr. Mody\u2019s and Mr. Gagnon\u2019s entering into employment with the company in accordance with Nasdaq Listing Rule 5635(c)(4). The RSUs will be subject to time-based vesting criteria, vesting in equal annual installments over four years.<\/p>\n

About Spruce Biosciences<\/b><\/p>\n

\nSpruce Biosciences is a late-stage biopharmaceutical company focused on developing and commercializing novel therapies for neurological disorders with significant unmet medical need. To learn more, visit www.sprucebio.com<\/a> and follow us on X<\/a>, LinkedIn<\/a>, Facebook<\/a> and YouTube<\/a>.<\/p>\n

Forward-Looking Statements<\/b><\/p>\n

\nStatements contained in this press release regarding matters that are not historical facts are \u201cforward-looking statements\u201d within the meaning of the Private Securities Litigation Reform Act of 1995. Such forward-looking statements include statements regarding, among other things, the impact of new management hires, the fulfillment of Spruce\u2019s strategic business objectives, the advancement and clinical execution of Spruce\u2019s drug development pipeline programs, and potential U.S. FDA approval. Because such statements are subject to risks and uncertainties, actual results may differ materially from those expressed or implied by such forward-looking statements. Words such as \u201cplans\u201d, \u201cwill\u201d, \u201cbelieve\u201d, \u201cpotential\u201d and similar expressions are intended to identify forward-looking statements. These forward-looking statements are based upon Spruce\u2019s current expectations and involve assumptions that may never materialize or may prove to be incorrect. Actual results could differ materially from those anticipated in such forward-looking statements as a result of various risks and uncertainties, which include, without limitation, risks and uncertainties associated with Spruce\u2019s business in general, the impact of geopolitical and macroeconomic events, and the other risks described in Spruce\u2019s filings with the U.S. Securities and Exchange Commission. All forward-looking statements contained in this press release speak only as of the date on which they were made and are based on management\u2019s assumptions and estimates as of such date. Spruce undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made, except as required by law.<\/p>\n

\"\"<\/p>\n

View source version on businesswire.com: <\/span>https:\/\/www.businesswire.com\/news\/home\/20260203184321\/en\/<\/a><\/span><\/p>\n

Media
\n<\/b>
Carolyn Hawley
\n
Inizio Evoke Comms
\n
Carolyn.Hawley@inizioevoke.com
\n<\/a>
media@sprucebio.com<\/a><\/p>\n

Investors
\n<\/b>
Samir Gharib
\n
President and CFO
\n
Spruce Biosciences, Inc.
\n
investors@sprucebio.com<\/a><\/p>\n

KEYWORDS:<\/b> California United States North America<\/p>\n

INDUSTRY KEYWORDS:<\/b> Biotechnology Neurology Health Pharmaceutical Clinical Trials<\/p>\n

MEDIA:<\/b><\/p>\n\n\n\n\n
Logo<\/b><\/font><\/td>\n<\/tr>\n
\"Logo\"<\/td>\n<\/tr>\n
<\/font><\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":"

Spruce Biosciences Adds Regulatory and Clinical Development Expertise to Leadership Team Daven Mody, Pharm.D., Appointed as Senior Vice President, Regulatory and Quality Bruno Gagnon, B.Pharm., M.Sc., Appointed as Senior Vice President, Clinical DevelopmentOperations SOUTH SAN FRANCISCO, Calif.–(BUSINESS WIRE)–Spruce Biosciences, Inc. (Nasdaq: SPRB), a late-stage biopharmaceutical company focused on developing and commercializing novel therapies for neurological disorders with significant unmet medical need, today announced the appointments of Daven Mody, Pharm.D., as Senior Vice President of Regulatory and Quality and Bruno Gagnon, B.Pharm., M.Sc., as Senior Vice President, Clinical Development Operations. \u201cWe are delighted to welcome both Daven and Bruno to the executive leadership team during a transformative time for Spruce,\u201d said Javier Scwarzberg, M.D., M.P.H., Chief Executive Officer of Spruce Biosciences. … <\/p>\n

Continue reading “Spruce Biosciences Adds Regulatory and Clinical Development Expertise to Leadership Team”<\/span><\/a><\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[],"tags":[],"class_list":["post-933568","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"\nSpruce Biosciences Adds Regulatory and Clinical Development Expertise to Leadership Team - Market Newsdesk<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.marketnewsdesk.com\/index.php\/spruce-biosciences-adds-regulatory-and-clinical-development-expertise-to-leadership-team\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Spruce Biosciences Adds Regulatory and Clinical Development Expertise to Leadership Team - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"Spruce Biosciences Adds Regulatory and Clinical Development Expertise to Leadership Team Daven Mody, Pharm.D., Appointed as Senior Vice President, Regulatory and Quality Bruno Gagnon, B.Pharm., M.Sc., Appointed as Senior Vice President, Clinical DevelopmentOperations SOUTH SAN FRANCISCO, Calif.–(BUSINESS WIRE)–Spruce Biosciences, Inc. (Nasdaq: SPRB), a late-stage biopharmaceutical company focused on developing and commercializing novel therapies for neurological disorders with significant unmet medical need, today announced the appointments of Daven Mody, Pharm.D., as Senior Vice President of Regulatory and Quality and Bruno Gagnon, B.Pharm., M.Sc., as Senior Vice President, Clinical Development Operations. \u201cWe are delighted to welcome both Daven and Bruno to the executive leadership team during a transformative time for Spruce,\u201d said Javier Scwarzberg, M.D., M.P.H., Chief Executive Officer of Spruce Biosciences. … Continue reading "Spruce Biosciences Adds Regulatory and Clinical Development Expertise to Leadership Team"\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.marketnewsdesk.com\/index.php\/spruce-biosciences-adds-regulatory-and-clinical-development-expertise-to-leadership-team\/\" \/>\n<meta property=\"og:site_name\" content=\"Market Newsdesk\" \/>\n<meta property=\"article:published_time\" content=\"2026-02-03T13:03:31+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/cts.businesswire.com\/ct\/CT?id=bwnews&sty=20260203184321r1&sid=flmnd&distro=nx&lang=en\" \/>\n<meta name=\"author\" content=\"Newsdesk\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Newsdesk\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"5 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/spruce-biosciences-adds-regulatory-and-clinical-development-expertise-to-leadership-team\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/spruce-biosciences-adds-regulatory-and-clinical-development-expertise-to-leadership-team\\\/\"},\"author\":{\"name\":\"Newsdesk\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/#\\\/schema\\\/person\\\/482f27a394d4fda80ecb5499e519d979\"},\"headline\":\"Spruce Biosciences Adds Regulatory and Clinical Development Expertise to Leadership Team\",\"datePublished\":\"2026-02-03T13:03:31+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/spruce-biosciences-adds-regulatory-and-clinical-development-expertise-to-leadership-team\\\/\"},\"wordCount\":1049,\"image\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/spruce-biosciences-adds-regulatory-and-clinical-development-expertise-to-leadership-team\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/cts.businesswire.com\\\/ct\\\/CT?id=bwnews&sty=20260203184321r1&sid=flmnd&distro=nx&lang=en\",\"inLanguage\":\"en-US\"},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/spruce-biosciences-adds-regulatory-and-clinical-development-expertise-to-leadership-team\\\/\",\"url\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/spruce-biosciences-adds-regulatory-and-clinical-development-expertise-to-leadership-team\\\/\",\"name\":\"Spruce Biosciences Adds Regulatory and Clinical Development Expertise to Leadership Team - 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