Welcome to our dedicated page for Relmada Therapeutics SEC filings (Ticker: RLMD), a comprehensive resource for investors and traders seeking official regulatory documents including 10-K annual reports, 10-Q quarterly earnings, 8-K material events, and insider trading forms.
Tracking Relmada Therapeutics’ path toward bringing esmethadone (REL-1017) to patients means reading dense SEC disclosures packed with clinical trial tables and R&D spend footnotes. Searching for when management raises capital, files an 8-K after a Phase 3 readout, or sells shares through Form 4 can feel like decoding a new molecule.
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Sergio Traversa, CEO and Director of Relmada Therapeutics, Inc. (RLMD), reported open-market purchases totaling 265,976 shares across three days, increasing his beneficial ownership to 1,000,000 shares. The Form 4 shows purchases on 08/26/2025 (80,545 shares at a weighted-average price of $0.62), 08/27/2025 (129,455 shares at $0.67), and 08/28/2025 (55,976 shares at $0.74). The filing explains each line represents aggregated open-market trades executed over price ranges: $0.61–$0.65, $0.65–$0.69, and $0.68–$0.79 respectively. All reported holdings are direct and the form is signed by the reporting person.
Schedule 13G/A filed for Relmada Therapeutics (RLMD) discloses beneficial ownership stakes held by Squadron-related filers. Squadron Master Fund LP reports shared beneficial ownership of 2,914,495 shares representing 8.8% of the outstanding common stock. Squadron Capital Management LLC and William Blank each report shared beneficial ownership of 3,298,500 shares, representing 9.9% of the class. The filing clarifies that Squadron Capital Management serves as adviser to funds that hold these shares and that Mr. Blank may be deemed to have investment and voting discretion, while expressly disclaiming beneficial ownership under Rule 13d-4. The ownership percentages are calculated using an issuer-stated share count of 33,191,622 shares outstanding.
Relmada Therapeutics, Inc. (NASDAQ: RLMD) filed a Form 8-K on 7-Aug-2025 announcing Item 2.02 (Results of Operations) and Item 7.01 (Reg FD).
- The company furnished, but did not file, a press release (Ex. 99.1) containing a corporate update and preliminary, unaudited Q2 2025 results for the period ended 30-Jun-2025.
- A conference call and webcast are scheduled for 7-Aug-2025 at 4:30 PM EDT to discuss the update.
- Full unaudited financial statements will appear in the forthcoming Form 10-Q.
- An updated corporate presentation (Ex. 99.2) was also furnished.
- No quantitative financial metrics, guidance, or transactional details are included in the 8-K itself; all figures reside in the referenced exhibits.
The furnished information is not deemed “filed” under the Exchange Act and therefore carries reduced liability. Investors must consult Exhibits 99.1 and 99.2 or the upcoming 10-Q for substantive financial data.
Relmada Therapeutics (RLMD) Q2-25 10-Q snapshot: The company remains pre-revenue and reported a Q2 net loss of $9.9 m (-44% YoY) and a 6-month loss of $27.4 m (-31% YoY) after sharply reducing R&D spend following the wind-down of its REL-1017 and psilocybin programs. Operating expenses fell 46% YoY to $10.2 m for the quarter.
Balance-sheet pressure intensified. Cash & cash equivalents dropped to $1.35 m (vs. $3.86 m YE-24) while short-term investments fell to $19.3 m (vs. $41.1 m), leaving $20.6 m of liquid resources. With $24.5 m operating cash burn in H1 and no revenue, management warns of substantial doubt about going-concern status.
Key corporate actions:
- Acquired Phase-2b-ready Sepranolone for €3 m cash.
- Licensed NDV-01 (Phase 2 NMIBC) for $3.5 m cash plus 3.0 m shares (≈10% dilution) and up to $200 m milestones; early Phase 2 data show 90% 6-month CR.
- Terminated esmethadone and psilocybin programs to focus resources on the new assets.
- Received Nasdaq bid-price deficiency notice; listing transferred to Nasdaq Capital Market with cure period to 19 Jan 2026.
Capital structure: Shares outstanding rose to 33.2 m (vs. 30.2 m YE-24); options outstanding 14.2 m; warrants 0.75 m. No ATM sales to date. Equity now stands at $15.9 m (vs. $35.5 m).
Outlook: Management is evaluating financing alternatives and may scale trial activity; upcoming catalysts include 9- and 12-month NDV-01 Phase 2 read-outs (2H-25) and planned IND for US trials in 1H-26.
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