Relmada Therapeutics/$RLMD

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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

RLMD Metrics

BasicAdvanced
$439M
-
-$0.85
0.49
-

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

NDV-01 generated encouraging 12-month Phase 2 interim results, including a 76% complete-response rate overall and 80% in BCG-unresponsive patients, with no Grade 3-or-higher treatment-related adverse events or treatment-related discontinuations reported. (Relmada Therapeutics)
Relmada reported $217.7 million in cash, cash equivalents and short-term investments as of June 30, 2026, which management expects to fund operations through 2029, including completion of the NDV-01 Phase 3 RESCUE program. (Relmada Therapeutics)
The pipeline offers multiple potential value drivers: NDV-01 is planned for two separate NMIBC indications, while sepranolone is targeted for Prader-Willi syndrome and other GABA-related disorders, with U.S. IND filings planned by year-end 2026. (SEC)
Relmada remains pre-revenue and loss-making: it reported a $32.0 million net loss and $24.7 million of operating cash burn for the six months ended June 30, 2026. (SEC)
The March 2026 $160.0 million PIPE materially increased the share count through 29.5 million new shares and 4.2 million pre-funded warrants, creating dilution for existing holders. (Relmada Therapeutics)
NDV-01 still faces substantial execution and regulatory risk: the company expects to file its U.S. IND by year-end 2026, with both Phase 3 programs dependent on FDA clearance, so pivotal development has not yet begun in the United States. (SEC)
Data summarised monthly by Lightyear AI. Last updated on 11 Sept 2026.

RLMD Financial Performance

Revenues and expenses
Income statement
QuarterlyAnnual
Q3 24
QoQ growth
Revenue
Net income
Profit margin

RLMD Earnings Performance

Company profitability
Earnings per share
QuarterlyAnnual
Q4 23
Q1 24
Q2 24
Q3 24
Q4 24
Actual
Expected
Surprise

Funds containing RLMD

Funds
Fund name
Fund size
$RLMD weighting
SPDR Russell 2000 US Small Cap€R2US
€4.8B0.01%
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