Relmada Therapeutics, Inc. (RLMD) Stock Price & How to Invest

Last updated July 2026

Short answer

Relmada Therapeutics (RLMD) is a small Nasdaq-listed biotech that rebuilt itself in 2025 around NDV-01, a sustained-release chemotherapy for bladder cancer, after its depression drug failed. At ~$3.39 a share it is a clinical-stage bet with ~$218 million of cash and no revenue, so the stock mostly moves on trial timing and data.

RLMD stock price

As of 2026-10-09, Relmada Therapeutics, Inc. (RLMD) last closed at $3.39, up 66.2% over the past year. Over the past 52 weeks it has traded between $1.93 and $7.86.

RLMD last close
$3.39
1 day
+6.94%
1 month
-17.11%
1 year
+66.18%
52-week range
$1.93 to $7.86
Last close
2026-10-09

Prices are daily closing prices from Yahoo Finance and may be delayed. For the live quote, check your broker or Relmada Therapeutics, Inc.'s investor relations page. Walnut is informational, not investment advice.

What does Relmada Therapeutics, Inc. (RLMD) do?

Relmada Therapeutics, Inc. is a clinical-stage biotechnology company based in Coral Gables, Florida, incorporated in Nevada and listed on the Nasdaq Capital Market. It has no approved products and has never generated revenue. Its two programs are NDV-01, a sustained-release formulation of the chemotherapy drugs gemcitabine and docetaxel that is placed directly into the bladder to treat non-muscle invasive bladder cancer (NMIBC), and sepranolone, a neurosteroid being developed first for Prader-Willi syndrome (PWS), with Tourette syndrome and essential tremor as possible later uses. It had 17 employees at the end of 2025 and relies on contract research and manufacturing firms.

The current company is the product of a turnaround. For most of its history Relmada was built around esmethadone (REL-1017), a drug for major depressive disorder. In December 2024 a planned interim analysis found the Reliance II pivotal trial was unlikely to succeed, and the stock collapsed. According to the 2026 proxy, the share price hit a low of 24 cents in March 2025, a market value of roughly $7 million. Management weighed a reverse merger and a wind-down, then chose to buy in new drug candidates instead. In February 2025 it bought sepranolone from Sweden's Asarina Pharma for €3 million, and in March 2025 it licensed NDV-01 from Israel's Trigone Pharma for $3.5 million upfront plus 3,017,420 shares (10% of the company at the time), with up to ~$200 million in milestones and a 3% royalty. The esmethadone license was terminated effective July 7, 2025, and a psilocybin program was ended in May 2025.

The money followed the data. After NDV-01 Phase 2 results, Relmada sold 40.1 million shares and pre-funded warrants at $2.20 in November 2025 (net proceeds ~$94 million), then raised ~$160 million gross in a March 2026 private placement at $4.75 a share, led by placement agents Jefferies, Leerink Partners, Piper Sandler and Mizuho. As of the March 2026 proxy, the largest holders were Janus Henderson (7.1%) and Squadron Capital Management (7.1%), with CEO Sergio Traversa at 5.8% and directors and officers together at 14.5%. Maged Shenouda is CFO, and Charles Casamento chairs the board. Bipin Dalmia joined as Chief Business Officer in July 2026, while the Chief Medical Officer for urology, Dr. Raj Pruthi, left on September 3, 2026. The stock joined the Russell 2000 on June 26, 2026.

The investment picture now turns on execution. Relmada held ~$217.7 million of cash and short-term investments on June 30, 2026, and says that funds operations through 2029, including the planned NDV-01 Phase 3 program. At ~$3.39 (October 9, 2026) and ~106.7 million shares, the market value is ~$362 million, meaning investors are paying roughly $145 million above net cash for the pipeline. The shares have fallen by more than half from their spring 2026 levels as timelines shifted: the March 2026 10-K expected initial Phase 3 data by year-end 2026, while the August update now targets only the IND filing by then, with Phase 3 starting after FDA clearance.

What's driving Relmada Therapeutics, Inc. (RLMD)?

1. NDV-01's Phase 2 results

The core of the story is a single-center Phase 2 trial in Israel in high-risk NMIBC. Among 48 patients dosed, 36 of 38 evaluable patients (95%) had a complete response at some point, and 19 of 25 (76%) were in complete response at 12 months, or 83% by Kaplan-Meier estimate. In the 20-patient BCG-unresponsive subgroup, the hardest-to-treat population, 8 of 10 evaluable patients (80%) were in complete response at 12 months. No patient progressed to muscle-invasive disease or needed bladder removal, and there were no grade 3 or higher treatment-related side effects. The main complaint was temporary painful urination. These are small, open-label numbers from one site.

2. The IND filing and Phase 3 RESCUE start

Relmada expects to file a US Investigational New Drug application for NDV-01 by year-end 2026 and to start the Phase 3 RESCUE program once the FDA clears it. After a Type B pre-IND meeting, the company says the FDA agreed on two studies: a single-arm trial in BCG-unresponsive, high-risk NMIBC with carcinoma in situ (primary endpoint: complete response at any time), and a randomized-to-observation trial in intermediate-risk patients after tumor removal (primary endpoint: disease-free survival). The FDA also agreed Relmada can lean on its prior safety findings for Gemzar and Taxotere under the 505(b)(2) pathway, which can cut non-clinical work. GMP manufacturing of clinical supply is underway, and management calls manufacturing its immediate priority. Whether the IND lands on schedule is the near-term catalyst most likely to move the stock.

3. Convenience as the selling point

Gemcitabine plus docetaxel is already used by urologists as an alternative to BCG, which has been in short supply globally since 2019. The drawback is logistics: conventional administration means sequential instillations over three to four hours. NDV-01 is designed to be given in under five minutes and to release both drugs inside the bladder for up to 10 days, keeping tumor exposure high while limiting absorption into the bloodstream. If that holds up, the pitch to busy urology practices is a familiar regimen in a far easier package.

4. Sepranolone in Prader-Willi syndrome

Sepranolone is designed to calm overactive GABA-A receptor signaling by acting on two receptor subtypes without directly blocking GABA. In a 12-week Phase 2a study in Tourette syndrome with 26 treated subjects, it reduced tic severity on the YGTSS scale by 28% versus standard care alone (p=0.051, just short of conventional significance) and improved several secondary measures. Across studies it has been tested in more than 335 participants without systemic side effects beyond injection-site reactions. Formulation is complete and the company is finalizing a pre-filled syringe; it targets an IND by year-end 2026 and then a Phase 2 proof-of-concept study in PWS.

5. Cash runway and spending

Relmada's balance sheet is unusually strong for its size. Cash and short-term investments were ~$217.7 million at June 30, 2026 against total liabilities of ~$12.5 million, and interest income alone was ~$2.3 million in the June quarter. Operating cash burn was ~$24.7 million in the first half of 2026, but spending will rise as Phase 3 trials start and drug manufacturing scales. Management says current funds last through 2029, which in principle covers RESCUE without new equity.

6. Patents and partnering

Relmada says it has more than 10 issued and pending patents on NDV-01 and more than 40 on sepranolone, with potential coverage beyond 2038. In April 2026 it filed a provisional US application on NDV-01 formulations that, if patents issue, could run to April 2047. The NDV-01 license covers the world excluding Israel, India and South Africa, and Trigone is owed up to ~$200 million in milestones plus a 3% royalty; a $2 million milestone was paid in January 2026. No partnering deal has been announced.

What are the risks to Relmada Therapeutics, Inc. (RLMD)?

The biggest risk is clinical: NDV-01's Phase 2 data come from 48 patients at a single site in Israel with no control arm, and response rates in small open-label studies often fall in larger multi-center trials. Timelines have already slipped, since the March 2026 10-K expected initial Phase 3 data by year-end 2026 while the August 2026 update targets only the IND filing by then, and manufacturing a novel sustained-release product is the step management itself flags as the gating item. The bladder cancer market is getting crowded, with approved or late-stage options from Johnson & Johnson, ImmunityBio, Ferring, CG Oncology and UroGen competing for the same urologists, so even an approved NDV-01 would need to win on convenience and durability. Relmada has no revenue, an accumulated deficit of ~$698 million at the end of 2025, and expects losses for the foreseeable future; any future raise would dilute holders, as the 2025 and 2026 financings already did, taking shares outstanding from about 33 million to about 107 million. Leadership turnover matters for a 17-person company, and the Chief Medical Officer for urology left in September 2026. Sepranolone's Tourette result missed statistical significance (p=0.051), and PWS has proven difficult for drug developers. Finally, RLMD is a small-cap stock that traded between ~$1.80 and $8.00 over the past year, so moves of 10% or more on little news are common.

What is the Relmada Therapeutics, Inc. (RLMD) forecast?

4 analysts publish price targets on RLMD, averaging $10.75 against a $3.39 price as of October 2026, or +217.1%. The published targets run from $9.00 to $12.00, a narrow spread, and the ratings split 4 buy, 0 hold, 0 sell. Over the last six months there have been 0 raises and 0 cuts among the published actions. A price target is what an analyst published on a date, not a prediction, and sell-side ratings skew positive across the whole market.

Read the full RLMD forecast and price target for the target table, the recent rating actions by firm, and how the consensus has shifted.

Is RLMD a buy or a sell?

We give no verdict on Relmada Therapeutics, Inc.. Both cases are real, which is why the question is contested at all, so here is the strongest version of each.

The case for buying. NDV-01's Phase 2 results. The core of the story is a single-center Phase 2 trial in Israel in high-risk NMIBC. The most optimistic published target, $12.00, assumes this works close to its best case.

The case against. The biggest risk is clinical: NDV-01's Phase 2 data come from 48 patients at a single site in Israel with no control arm, and response rates in small open-label studies often fall in larger multi-center trials. The most pessimistic target, $9.00, is roughly what RLMD is worth if this bites instead.

Read the full bull and bear case on RLMD, including what would have to change to break either one. Walnut is not an investment adviser.

How is Relmada Therapeutics, Inc. (RLMD) valued? (approximate, October 2026)

A simple financial snapshot. These are approximations and refresh quarterly; for current figures see Relmada Therapeutics, Inc.'s investor relations page or your broker.

  • Revenue (TTM): $0 (no approved products)
  • Net loss (H1 2026): ~$32.0 million
  • Net loss (FY 2025): ~$57.4 million
  • Cash + short-term investments (Jun 30, 2026): ~$217.7 million
  • Shares outstanding (Aug 4, 2026): ~106.7 million (+5.8M pre-funded warrants)
  • Market cap (Oct 9, 2026): ~$362 million at ~$3.39

With no revenue, the usual earnings ratios do not apply. The useful comparison is market value against cash: at ~$362 million versus ~$218 million of cash and investments, the market assigns roughly $145 million to NDV-01, sepranolone and the team. Quarterly losses of ~$13 million are modest for a company preparing a Phase 3 program, and interest income is offsetting part of the spend. That premium was far larger in spring 2026, when the shares traded above $7. The next quarterly report, expected in November based on last year's calendar, should show whether spending is ramping as planned.

Who competes with Relmada Therapeutics, Inc. (RLMD)?

BCG-unresponsive bladder cancer therapies

Johnson & Johnson's TAR-200 (Inlexzo), a gemcitabine-releasing bladder device, is the closest conceptual rival because it also delivers chemotherapy over days inside the bladder. ImmunityBio's Anktiva, Ferring's Adstiladrin gene therapy and Merck's Keytruda are already used in BCG-unresponsive disease, and CG Oncology's cretostimogene and enGene's detalimogene are in late-stage development.

Intermediate-risk and recurrent NMIBC

UroGen Pharma's mitomycin-based products, including Zusduri for recurrent low-grade intermediate-risk disease, target the setting of NDV-01's planned adjuvant trial. Conventional sequential gemcitabine and docetaxel instillations, given off-label by urologists, are the standard NDV-01 is trying to simplify.

Prader-Willi syndrome

Soleno Therapeutics' Vykat XR (diazoxide choline) is approved for hyperphagia in PWS, and Acadia Pharmaceuticals and Harmony Biosciences have run programs in the condition. Sepranolone would enter a field where several mechanisms have been tried with mixed results.

Tourette syndrome

Emalex Biosciences' ecopipam is the most advanced new Tourette drug candidate, and older antipsychotics are used today. Sepranolone's Tourette data would have to compete with both if Relmada returns to that indication.

What stocks are similar to Relmada Therapeutics, Inc. (RLMD)?

Other names that sit close to RLMD: same theme, named as a direct competitor, or held beside it in the same funds. Each entry says which. Worth a look if you are thinking about diversification within a thesis rather than concentration on one ticker.

How to invest in Relmada Therapeutics, Inc. (RLMD)

There are three common ways to get RLMD exposure. Buy shares (or fractional shares) directly at any major broker. Hold an ETF that includes it, which spreads the position across many companies. Or build it into a focused thematic portfolio, so RLMD sits alongside other stocks that express the same thesis.

Walnut takes the portfolio route. Describe a thesis where RLMD fits (for example “AI infrastructure” or “dividend-growth large-caps”) and the AI proposes 5 to 6 constituents with target weights. You review the plan and fund it through your own broker when you're ready.

New to this? Start with how to invest in stocks, see how to analyze a stock with AI, or compare the best AI stock analyzers.

The bottom line on Relmada Therapeutics, Inc. (RLMD)

RLMD is a well-funded, pre-revenue wager that NDV-01 can turn strong single-center Phase 2 results into a registrational win in a crowded bladder cancer market, with sepranolone as a smaller second shot.

More on Relmada Therapeutics, Inc. (RLMD)

Whether RLMD is worth buying today depends more on your time horizon and what you already hold than on any single call. We walk through valuation, what would have to go right, and the risks in is RLMD a buy or a sell?, and where the stock could go from here in the RLMD stock forecast.

For income investors, whether RLMD pays a dividend and how the payout looks is covered in does RLMD pay a dividend? And to weigh RLMD against a peer, read the full side-by-side comparisons: RLMD vs JNJ and RLMD vs IBRX.

Wondering how RLMD fits the portfolio you already own? Walnut is an AI investing app that connects your brokerage read-only and answers questions like that about your actual holdings: overlap, concentration, and how each position tracks the S&P 500. Compare the best AI portfolio analyzers or see the best AI investing apps in 2026.

Investing in Relmada Therapeutics, Inc. with AI

Connect the broker you already use and ask Walnut's AI how RLMD fits what you actually hold: whether you own it already through a fund, what it would do to your concentration, and how it has tracked the S&P 500. Read-only by default, and you approve anything before it reaches your broker.

FAQ

What does Relmada Therapeutics do?

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Relmada is a clinical-stage biotech developing two drugs: NDV-01, a sustained-release form of the chemotherapy pair gemcitabine and docetaxel for non-muscle invasive bladder cancer, and sepranolone, a neurosteroid aimed first at Prader-Willi syndrome. It has no approved products and no revenue. It is based in Coral Gables, Florida, and had 17 employees at the end of 2025.

Why did RLMD stock crash in 2024?

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In December 2024 an interim analysis showed that Reliance II, the pivotal trial of Relmada's depression drug esmethadone (REL-1017), was unlikely to meet its main goal. The stock fell from about $3 to under $1 and hit a low of 24 cents in March 2025, according to the company's proxy. Relmada later ended the esmethadone program, effective July 2025.

Why did RLMD stock rise in 2025?

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The rebound came from the new pipeline. Relmada licensed NDV-01 in March 2025, and Phase 2 data showing high complete-response rates in high-risk bladder cancer drew investor interest. The company then raised ~$94 million at $2.20 a share in November 2025 and ~$160 million gross at $4.75 in March 2026, and the shares traded above $7 in spring 2026 before falling back.

Does Relmada pay a dividend?

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No. Relmada has never paid a dividend and, as a pre-revenue biotech that lost ~$57 million in 2025 and ~$32 million in the first half of 2026, it puts its cash into clinical development. Any return for shareholders would come from the share price, which depends on trial results, regulatory progress and any partnering deals.

When does Relmada report earnings?

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Relmada reports quarterly with a 10-Q and press release. It reported second-quarter 2026 results on August 6, 2026, and reported the comparable quarter last year on November 13, 2025, so third-quarter 2026 results are likely in mid-November 2026. Full-year results come in March.

Who owns Relmada Therapeutics?

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Per the 2026 proxy, Janus Henderson Group and Squadron Capital Management each held about 7.1% as of March 2026. CEO Sergio Traversa owned about 5.8% including options, and all directors and executive officers together held about 14.5%. Trigone Pharma also received about 3 million shares in the NDV-01 deal.

How much cash does Relmada have?

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Relmada held ~$217.7 million in cash, cash equivalents and short-term investments on June 30, 2026, up from ~$93 million at the end of 2025 after the March 2026 private placement. Management says that funds operations through 2029, including completion of the planned NDV-01 Phase 3 RESCUE program. Total liabilities were ~$12.5 million.

When will NDV-01 start Phase 3?

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Relmada expects to file the NDV-01 Investigational New Drug application with the FDA by year-end 2026 and to begin the Phase 3 RESCUE program after the FDA clears it. RESCUE has two studies: a single-arm trial in BCG-unresponsive high-risk NMIBC with carcinoma in situ, and a randomized-to-observation trial in intermediate-risk patients in the adjuvant setting.

Is RLMD a penny stock?

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Not currently. It traded below $1 for much of the first half of 2025 after the esmethadone failure, but it has been above $1 since late summer 2025 and closed around $3.39 on October 9, 2026. With a market value of roughly $362 million and Russell 2000 membership since June 2026, it is a small-cap biotech, though still volatile.

How do I buy RLMD stock in the US?

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RLMD trades on the Nasdaq Capital Market, so it is available at most US brokers, including Fidelity, Schwab, Robinhood, E*Trade and Public. You search the ticker RLMD and place an order like any other US stock.

Who makes NDV-01 and who owns its rights?

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NDV-01 was developed by Trigone Pharma, a private Israeli company. Relmada licensed exclusive worldwide rights, except in Israel, India and South Africa, in March 2025. Relmada owes Trigone up to ~$200 million in development, regulatory and commercial milestones plus a 3% royalty on sales, and paid a $2 million milestone in January 2026.

Walnut is informational, not investment advice. Financial figures on this page are approximations; always verify current numbers with Relmada Therapeutics, Inc.'s investor relations page or your broker before making investment decisions.