Relmada Therapeutics/$RLMD
1D1W1M3M6MYTD1Y5YMAX
Capital at risk
About Relmada Therapeutics
Relmada Therapeutics Inc is a clinical-stage, publicly traded biotechnology company focused on the development of NDV-01 and sepranolone. NDV-01 is a novel, controlled-release intravesical formulation of gemcitabine and docetaxel. NDV-01 is currently in a Phase 2 clinical trial in Isreal to assess its safety and efficacy in patients with aggressive forms of non-muscle invasive bladder cancer (NMIBC). Sepranolone is a novel neurosteroid epimer of allopregnanolone. sepranolone is being developed for the potential treatment of Prader-Willi Syndrome, Tourette Syndrome, excessive tremor and other diseases related to excessive GABAergic activity.
- Ticker
- $RLMD
- Sector
- Health
- Primary listing
- NASDAQ
- Employees
- 17
- Headquarters
- Coral Gables, United States
- Website
- www.relmada.com
RLMD Metrics
BasicAdvanced
$473M
-
-$0.85
0.49
-
Price and volume
Market cap
$473M
Beta
0.49
52-week high
$8.00
52-week low
$3.07
Average daily volume
1.6M
Financial strength
Current ratio
29.517
Quick ratio
29.342
Profitability
Management effectiveness
Return on assets (TTM)
-32.39%
Return on equity (TTM)
-55.66%
Valuation
Price to book
2.29
Price to tangible book (TTM)
2.29
Price to free cash flow (TTM)
-7.055
Free cash flow yield (TTM)
-14.18%
Free cash flow per share (TTM)
-0.628
Growth
Earnings per share change (TTM)
-61.36%
3-year earnings per share growth (CAGR)
-41.81%
What the Analysts think about RLMD
Analyst ratings (Buy, Hold, Sell) for Relmada Therapeutics stock.
Analyst projections of the future price of Relmada Therapeutics stock.
Bulls say / Bears say
In the Phase 2 study, NDV-01 produced a complete response at some point in 95% of efficacy-evaluable patients, with 76% still in response at 12 months. Relmada also reported no severe treatment-related events, supporting further testing of the bladder-cancer candidate. (Relmada Therapeutics)
The FDA has aligned with Relmada on two registrational development pathways for NDV-01, covering different NMIBC patient groups. If manufacturing and regulatory steps are completed, the programme could address more than one treatment setting. (Relmada Therapeutics)
Relmada reported $217.7 million in cash and short-term investments at the end of June, which it expects to fund operations through 2029, including the NDV-01 Phase 3 programme. That gives the company time to pursue its main clinical catalyst without an immediate funding need, based on management’s forecast. (Relmada Therapeutics)
NDV-01’s US IND and Phase 3 start moved from a mid-2026 target to an IND filing expected by year-end, as manufacturing work remains underway. This makes progress dependent on successful GMP scale-up and leaves room for further delays. (Relmada Therapeutics, Relmada Therapeutics)
The encouraging NDV-01 results come from an open-label, single-arm Phase 2 study, rather than a controlled comparison. Only 25 efficacy-evaluable patients had 12-month data, so the response rate may not predict results in larger registrational trials. (SEC)
Relmada’s March 2026 private placement issued about 29.5 million shares and included pre-funded warrants for a further 4.2 million shares. That large equity raise diluted existing holders, even though it strengthened the company’s cash position. (SEC)
Data summarised monthly by Lightyear AI. Last updated on 20 Oct 2026.
RLMD Financial Performance
Revenues and expenses
RLMD Earnings Performance
Company profitability
Upcoming events
No upcoming events
Funds containing RLMD
Fund name | Fund size | $RLMD weighting |
|---|---|---|
SPDR Russell 2000 US Small Cap€R2US | $5B | 0.01% |
SPDR Russell 2000 US Small Cap£R2SC | $5B | 0.01% |
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