Relmada Therapeutics (RLMD) Corporate presentation summary
Event summary combining transcript, slides, and related documents.
Corporate presentation summary
19 Mar, 2026Investment highlights and pipeline
NDV-01, a sustained-release gemcitabine/docetaxel therapy, leads a pipeline targeting non-muscle invasive bladder cancer (NMIBC) with a well-defined regulatory path and strong commercial potential.
NDV-01 offers improved administration speed, extended tumor exposure, and physician familiarity compared to conventional therapies.
The pipeline includes multiple late-stage studies for NDV-01 in various NMIBC risk groups and Sepranolone for Prader-Willi syndrome.
Leadership team has deep expertise in urology and clinical development.
Market opportunity and disease landscape
NMIBC represents 80% of new bladder cancer cases, with high recurrence rates and a $6.5B annual U.S. treatment cost.
Recurrence and progression risks are significant, especially for intermediate- and high-risk patients.
Current treatments involve complex pathways, frequent invasive procedures, and substantial patient burden.
NDV-01 product profile and advantages
NDV-01 is a ready-to-use, office-based therapy administered in under 5 minutes, enabling broader community adoption.
Provides sustained intravesical drug release for up to 10 days, enhancing tumor exposure and reducing administration frequency.
Biodegradable polymer ensures safe excretion, avoiding device extraction required by some competitors.
Demonstrates stable, predictable drug levels in vitro, minimizing systemic side effects.
Latest events from Relmada Therapeutics
- NDV-01 shows strong efficacy and safety in bladder cancer, with pivotal trials and funding secured.RLMD
Leerink Global Healthcare Conference 202628 Mar 2026 - NDV-01 phase II shows 76% 12-month CR and $160M financing supports phase III launch.RLMD
Q4 202520 Mar 2026 - NDV-01 achieved durable, high response rates with favorable safety in high-risk NMIBC.RLMD
Study Result Presentation19 Mar 2026 - NDV-01 and sepranolone advance toward pivotal studies, supported by strong clinical and financial positions.RLMD
Investor presentation10 Mar 2026 - Q2 net loss narrowed, cash supports late-stage CNS trials and key milestones into 2025.RLMD
Q2 20242 Feb 2026 - Relight trial aims for robust efficacy in MDD with improved design and strict patient selection.RLMD
Goldman Sachs 45th Annual Global Healthcare Conference1 Feb 2026 - Phase III data for REL-1017 in adjunctive depression is expected in H2 2024, with NDA filing possible in 2025.RLMD
Jefferies 2024 Global Healthcare Conference1 Feb 2026 - Q3 net loss was $21.7M; phase III interim analysis and liquidity concerns remain key.RLMD
Q3 202415 Jan 2026 - Late-stage MDD trial nears interim data, with improved design and strong financial runway.RLMD
Jefferies London Healthcare Conference13 Jan 2026