Relmada Therapeutics Appoints Urology Expert Raj S. Pruthi, MD as CMO-Urology
Appointment of Dr. Raj S. Pruthi: Relmada Therapeutics has appointed Dr. Raj S. Pruthi as Chief Medical Officer-Urology, bringing over 25 years of experience in urologic oncology and clinical trials to advance the development of their lead program, NDV-01, for non-muscle invasive bladder cancer (NMIBC).
NDV-01 Development Timeline: The Phase 3 trial for NDV-01 is expected to commence in the first half of 2026, following positive initial Phase 2 data presented at the American Urology Association 2025 Annual Meeting, highlighting its potential as a leading therapy for NMIBC with favorable tolerability and ease of administration.
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Offering Details: Relmada Therapeutics announced the pricing of an underwritten offering of 40,142,000 shares of common stock at $2.20 per share, along with pre-funded warrants for an additional 5,315,000 shares, aiming to raise approximately $100 million before expenses.
Use of Proceeds: The funds will be utilized for working capital, clinical studies for regulatory approvals, development of product candidates, and potential acquisitions or licensing of complementary technologies.
Investor Participation: Notable investors in the offering include Janus Henderson Investors, Ferring Ventures SA, and OrbiMed, with Jefferies and Leerink Partners serving as joint book-running managers.
Forward-Looking Statements: The announcement includes forward-looking statements regarding the offering's completion and intended use of proceeds, highlighting the inherent risks and uncertainties involved.

FDA Feedback on NDV-01: Relmada Therapeutics received positive feedback from the FDA regarding the planned Phase 3 trials for NDV-01 in non-muscle invasive bladder cancer (NMIBC), confirming no additional non-clinical studies are needed and supporting two potential registrational trials.
Efficacy and Safety Data: The 9-month follow-up data for NDV-01 showed a 92% overall response rate in NMIBC patients, with no progression to muscle invasive disease and no new safety signals reported.
Clinical Trial Design: The FDA indicated that a single-arm trial may be acceptable for high-grade, 2nd line BCG-unresponsive NMIBC patients, while a randomized controlled trial is acceptable for intermediate-risk NMIBC patients.
Market Potential: NDV-01, a sustained-release formulation of gemcitabine and docetaxel, aims to address the significant unmet needs in NMIBC, which represents 75-80% of bladder cancer cases and has limited treatment options.

Appointment of Dr. Max Kates: Dr. Max Kates has been appointed to Relmada Therapeutics' Clinical Advisory Board to support the development of NDV-01, a treatment for non-muscle invasive bladder cancer (NMIBC), with the Phase 3 program expected to start in H1 2026.
Significance of NDV-01: NDV-01 is a sustained-release formulation of gemcitabine and docetaxel designed for intravesical administration, aiming to improve treatment outcomes for NMIBC, which accounts for 75-80% of bladder cancer cases and has high recurrence rates.
Relmada Therapeutics Insider Purchase: CEO Sergio Traversa bought 265,976 shares of RLMD for $178,095, currently seeing a 119.5% gain as the stock trades at $1.47, up 26.8% on Tuesday.
Strategic Education Insider Purchase: CFO Daniel Wayne Jackson purchased 1,900 shares of Strategic Education for $154,850, with the stock up 0.6% on Tuesday.

Management Insights: Relmada Therapeutics is advancing two promising product candidates, NDV-01 for bladder cancer and sepranolone for compulsivity disorders, with plans to initiate Phase III and proof-of-concept studies in 2026. The company reported a decrease in operational costs and a net loss of $9.9 million for Q2 2025, while emphasizing the importance of regulatory engagement and strategic financial management.
Analyst Sentiment: Analysts expressed a slightly positive outlook on the company's progress, highlighting encouraging efficacy data and seeking clarity on market strategies and regulatory pathways. Management maintained a confident tone during the earnings call, focusing on upcoming milestones and the potential for both products to address significant unmet medical needs.






