Relmada Therapeutics
Relmada Therapeutics is a clinical-stage biotechnology company developing NDV-01, a sustained-release intravesical formulation for non-muscle invasive bladder cancer, and sepranolone, a GABA-A receptor modulator for CNS disorders including Prader-Willi syndrome, Tourette syndrome, and OCD.
- Company typePublic
- Founded2013
- HeadquartersNew York, United States
- Headcount11–50
- GTM typeB2B
- OfferingHardware or Manufacturing
What Relmada Therapeutics does
Relmada Therapeutics is a clinical-stage biotechnology company developing therapies for oncology and central nervous system disorders, traded on NASDAQ under ticker RLMD and headquartered in Coral Gables, Florida. Its lead asset, NDV-01, is a sustained-release intravesical formulation of gemcitabine and docetaxel (Gem/Doce) engineered for non-muscle invasive bladder cancer (NMIBC); the formulation enables approximately 10 days of controlled local drug release and in-office administration in under 5 minutes without anesthesia. NDV-01 reported 76% complete response at 12 months and 95% CR at any time in high-risk NMIBC patients, with 80% CR at 12 months in BCG-unresponsive disease and no observed progression to muscle-invasive disease; the program has FDA alignment on two registrational pathways (2L BCG-unresponsive and adjuvant intermediate-risk) and is advancing into the Phase 3 RESCUE registrational trial expected to initiate mid-2026. A provisional patent filed in April 2026 could extend exclusivity through 2047 if granted.
The company's second program, sepranolone, is a synthetic isoallopregnanolone that selectively antagonizes allopregnanolone at GABA-A receptors without broadly disrupting GABAergic signaling; it targets compulsive behaviors in Prader-Willi syndrome, Tourette syndrome, and OCD, with a Phase 2 trial in Prader-Willi expected mid-2026. Both assets were in-licensed or acquired in 2025 (NDV-01 from Trigone Pharma; sepranolone from Sweden-based Asarina Pharma AB), marking a strategic pivot following prior Phase 3 setbacks with REL-1017 in major depressive disorder. The business model is pre-revenue: there are no approved products and no product sales, and the company funds operations through equity financings — approximately $410M raised across a December 2021 $150M public offering, a November 2025 $100M offering, and a March 2026 $160M PIPE with RA Capital, OrbiMed, Janus Henderson, and Venrock. The company reported $234M in cash as of March 31, 2026, with management stating runway through 2029, a $57.4M net loss for full-year 2025, and a Q1 2026 net loss of $19.1M. Future commercialization of NDV-01 is planned through specialty pharmacy networks serving academic and community urology practices.
Relmada Therapeutics firmographics
Firmographics- Name
- Relmada Therapeutics
- Legal name
- Relmada Therapeutics, Inc.
- Website
- https://relmada.com
- Company type
- Public
- Founded year
- 2013
- Operating status
- Operating
- Headcount range
- 11–50 employees
- Short description
- Relmada Therapeutics is a clinical-stage biotechnology company developing NDV-01, a sustained-release intravesical formulation for non-muscle invasive bladder cancer, and sepranolone, a GABA-A receptor modulator for CNS disorders including Prader-Willi syndrome, Tourette syndrome, and OCD.
- Ownership category
- akta.pro rank
Relmada Therapeutics industry classification
Industry- Product category
- Biopharmaceuticals
- NAICS
- Scientific Research and Development Services (5417)
- SIC
- Pharmaceutical Preparations (2834)
- akta.pro primary industry
- Oncology Gene Therapies (incl. oncolytic vectors & gene-modified approaches) (HLAAACAF)
- akta.pro secondary industry
- Gene Therapy for Rare/Monogenic Diseases (HLAAACAE)
Keywords
Where Relmada Therapeutics is headquartered
LocationHeadquarters
- HQ city
- New York
- HQ country
- United States
- HQ region
- North America
Offices1 record
Markets served
Relmada Therapeutics business model
Business model- GTM type
- B2B
- Offering type
- Hardware or Manufacturing
- Cost components
- Technology or R&D, Personnel, Operations, Marketing or Sales
Revenue model
- Pharmaceutical Product Revenue: Pre-revenue clinical-stage biotechnology company. Intends to commercialize NDV-01 for non-muscle invasive bladder cancer and sepranolone for CNS disorders including Prader-Willi syndrome, Tourette syndrome, and OCD upon regulatory approval.
Go-to-market motion1 record
Distribution channels1 record
Marketing channels4 records
Relmada Therapeutics product offering
Product offeringCore offering
Relmada Therapeutics is a clinical-stage biotechnology company developing two lead product candidates: NDV-01, a sustained-release intravesical formulation of gemcitabine and docetaxel for non-muscle invasive bladder cancer (NMIBC) advancing toward a Phase 3 registrational program, and Sepranolone, a GABAA receptor modulator targeting compulsive behaviors in CNS disorders including Prader-Willi syndrome, Tourette syndrome, and OCD. The company has no approved or commercial products and is pre-revenue.
Product overview
Relmada Therapeutics is a clinical-stage biotechnology company developing two lead product candidates: NDV-01, a sustained-release intravesical formulation of gemcitabine and docetaxel for non-muscle invasive bladder cancer advancing into Phase 3 trials, and sepranolone, a GABAA receptor modulator targeting compulsive behaviors in CNS disorders including Prader-Willi syndrome. The company focuses on oncology and central nervous system disorders with an emphasis on delivering durable efficacy, favorable safety, and real-world usability.
Differentiator
Problem solved
Functional benefit
Products and services
- NDV-01 A sustained-release intravesical formulation of gemcitabine and docetaxel (Gem/Doce) for the treatment of non-muscle invasive bladder cancer (NMIBC). Engineered for prolonged bladder retention and controlled drug release over approximately 10 days, enabling streamlined in-office administration in under 5 minutes without anesthesia or specialized equipment. Targets high-risk NMIBC patients who failed BCG therapy and intermediate-risk NMIBC patients in adjuvant setting.
- Sepranolone A synthetic isoallopregnanolone that selectively antagonizes allopregnanolone (ALLO) at GABA-A receptors without disrupting general GABA signaling. Targets disorders linked to excess GABAergic activity including Prader-Willi syndrome, Tourette syndrome, and obsessive-compulsive disorder (OCD). Prior clinical and preclinical data support effects on food craving, appetite and compulsive behaviors.
Quantifiable outcome
- 76% complete response rate at 12 months in high-risk NMIBC patients
- +4 more outcomes
Companies that use Relmada Therapeutics
Customer profileSegments2 records
Ideal customer profiles2 records
Relmada Therapeutics technology and API
TechnologyTechnology focussed Yes
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Feature2 records
Relmada Therapeutics partnerships and signals
Strategic signalPartnerships
Five partnerships are on record, tiered core, key advisor and investor relations.
- Asarina Pharma ABcoreRelmada acquired sepranolone, a Phase 2b-ready neurosteroid targeting GABA-A receptors, from Sweden-based Asarina Pharma AB in February 2025. Sepranolone targets compulsive behaviors for disorders including Prader-Willi syndrome, Tourette syndrome, and OCD. The acquisition expanded Relmada's CNS disorder portfolio.
- Trigone Pharma Ltd.coreRelmada licensed NDV-01, a Phase 2 bladder cancer candidate, from Trigone Pharma. NDV-01 is a sustained-release intravesical formulation of gemcitabine and docetaxel for non-muscle invasive bladder cancer. This license agreement was key to Relmada's strategic pivot into oncology.
- Michael Quirk, PhDkey advisorAppointed as Senior Advisor for sepranolone program in June 2026. Dr. Quirk brings over 20 years of neuroscience drug discovery experience, having served as Chief Scientific Officer and interim Head of R&D at Sage Therapeutics.
- Raj S. Pruthi, MDkey advisorChief Medical Officer of Relmada Therapeutics - Urology. Appointed to lead development of cancer treatment programs. Also serves on PreveCeutical Medical's board.
- LifeSci Advisorsinvestor relationsInvestor relations contact for Relmada. Brian Ritchie from LifeSci Advisors serves as the primary IR contact for the company.
Scale indicators8 records
Recent moves6 records
Expansion highlights6 records
Relmada Therapeutics competitors and assessment
Company assessmentDirect peers
- Marinus Pharmaceuticals: Developer of Ztalmy (ganaxolone), a neurosteroid acting on GABA-A receptors approved for seizures associated with CDKL5 deficiency disorder. Direct CNS neurosteroid peer comparable to sepranolone's GABA-A mechanism.
- CG Oncology: Clinical-stage biotech developing cretostimogene, an intravesical gene therapy for BCG-unresponsive NMIBC. Directly comparable to Relmada's NDV-01 program targeting the same patient population with overlapping treatment settings.
- ImmunityBio: Developer of Anktiva (nogapendekin alfa), an IL-15 superagonist approved for BCG-unresponsive NMIBC. Direct competitor to NDV-01 in the same NMIBC treatment space with established regulatory and commercial footprint.
- Ferring Pharmaceuticals: Developer of Adstiladrin (nadofaragene), an intravesical gene therapy approved for BCG-unresponsive NMIBC. Direct competitor to NDV-01 with similar mechanism of local bladder delivery in the same indication.
- Sage Therapeutics: Developer of Zurzuvae (zuranolone), a neurosteroid acting on GABA-A receptors approved for postpartum depression. Closely comparable to sepranolone's GABA-A modulation mechanism; Senior Advisor Michael Quirk joined Relmada from Sage.
Broad incumbents
- Merck & Co. Large pharmaceutical company with KEYTRUDA (pembrolizumab) approved for BCG-unresponsive NMIBC. Competes with NDV-01 in the same indication but as part of a broader oncology portfolio rather than a focused NMIBC asset.
- Bristol Myers Squibb: Major oncology incumbent with Opdivo and a broad bladder cancer franchise. Competes in NMIBC and broader oncology but is a broad-line pharmaceutical player rather than a focused biotech.
- Johnson & Johnson: Diversified healthcare incumbent with significant oncology and CNS franchises. Represents the strategic acquirer profile relevant to clinical-stage biotechs like Relmada, though not a direct product competitor in NMIBC.
- Pfizer: Large pharmaceutical company with deep oncology and CNS pipelines. Relevant as a potential strategic acquirer and broad industry peer, but does not directly compete in NMIBC or sepranolone's CNS indications.
Others
- Asarina Pharma: Swedish biotech from which Relmada acquired sepranolone in February 2025. Adjacent technology originator with prior expertise in sepranolone's GABA-A mechanism for CNS disorders.
Market position
Strengths4 records
Weaknesses4 records
Competitive moat3 records
Key risks6 records
Key highlights7 records
Customer concentration
Relmada Therapeutics social profiles
Digital presenceRelmada Therapeutics financial estimates
Financial estimateRevenue estimate
Valuation estimate
Relmada Therapeutics leadership team
Management profileNumber of profiles
Profiles7 records
Relmada Therapeutics funding detail
Funding detailFunding overview
Funding rounds12 records
Investors18 records
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
Relmada Therapeutics M&A and investment
M&A and investmentM&A
Investments
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about Relmada Therapeutics
What does Relmada Therapeutics do?
Relmada Therapeutics is a clinical-stage biotechnology company developing two lead product candidates: NDV-01, a sustained-release intravesical formulation of gemcitabine and docetaxel for non-muscle invasive bladder cancer (NMIBC) advancing toward a Phase 3 registrational program, and Sepranolone, a GABAA receptor modulator targeting compulsive behaviors in CNS disorders including Prader-Willi syndrome, Tourette syndrome, and OCD. The company has no approved or commercial products and is pre-revenue.
Is Relmada Therapeutics a public or private company?
Relmada Therapeutics is a public company. It is classified as public and is currently operating.
When was Relmada Therapeutics founded?
Relmada Therapeutics was founded in 2013. It employs 11 to 50 people.
Where is Relmada Therapeutics based?
Relmada Therapeutics is headquartered in New York, United States, in the North America region.
How does Relmada Therapeutics make money?
One revenue line is on record: pharmaceutical Product Revenue.
Who are Relmada Therapeutics's main competitors?
Direct peers on record are Marinus Pharmaceuticals, CG Oncology, ImmunityBio, Ferring Pharmaceuticals and Sage Therapeutics. Broad incumbents are Merck & Co., Bristol Myers Squibb, Johnson & Johnson and Pfizer. Asarina Pharma is listed as an others.
Does Relmada Therapeutics have an API?
No public API is recorded for Relmada Therapeutics.
What industry is Relmada Therapeutics in?
Relmada Therapeutics's product category is Biopharmaceuticals. Its primary akta.pro industry code is HLAAACAF, Oncology Gene Therapies (incl. oncolytic vectors & gene-modified approaches), with a secondary code of HLAAACAE, Gene Therapy for Rare/Monogenic Diseases. Its NAICS code is 5417 and its SIC code is 2834.