RLMD Relmada Therapeutics
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Executive Summary
Relmada Therapeutics reported financial results for 2025 and provided a corporate update highlighting positive 12-month Phase 2 data for NDV-01 in non-muscle invasive bladder cancer (NMIBC), showing a 76% durable complete response rate and favorable safety. The company secured $160 million in PIPE financing in March 2026, boosting its cash runway through 2029 to fund the upcoming Phase 3 RESCUE program. Despite a reduced net loss, the company remains pre-revenue with no near-term earnings inflection.
Key Financial Metrics
Actionable Insight
Investors should monitor initiation of the Phase 3 RESCUE program in mid-2026 and initial 3-month NDV-01 data from the 2L BCG-unresponsive study expected by year-end 2026. The combination of strong Phase 2 durability, clean safety profile, and extended funding significantly de-risks near-term development and increases probability of regulatory success.
Key Facts
- NDV-01 Phase 2 data shows 76% complete response (CR) rate at 12 months and 95% CR at any time in high-risk NMIBC; 80% CR at 12 months in BCG-unresponsive patients
- No Grade ≥3 treatment-related adverse events or treatment discontinuations observed
- FDA alignment confirmed on two registrational pathways for NDV-01: adjuvant intermediate-risk NMIBC and 2L BCG-unresponsive NMIBC
- Oversubscribed $160 million PIPE financing completed in March 2026, led by top healthcare investors
- Cash balance of $93.0 million as of December 31, 2025, now expected to fund operations through 2029 including Phase 3 development
- Phase 3 RESCUE program initiation expected mid-2026; U.S. IND clearance also anticipated mid-2026
- Net loss for 2025 was $57.4 million ($1.45/share), improved from $80.0 million ($2.65/share) in 2024
Financial Impact
Cash runway extended to 2029 with $253M total liquidity (existing $93M + $160M PIPE); R&D spend decreased 42% YoY to $26.9M due to completion of prior trials
Risk Factors
- Phase 3 trial may not replicate Phase 2 efficacy or safety results
- Regulatory delays or failure to maintain alignment with FDA on trial design
- Dilution risk from future financings if additional capital is needed beyond 2029
Market Snapshot
Documents Analyzed
This report is based on 1 press release from GlobeNewswire.
| Document | Accession Number |
|---|---|
| PRESS-RELEASE Data (Synthetic) | press-3259417 |
Track record builds as more directional reports settle.
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May 13, 2026
27d ago
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S-3ASR
| $7.42 $7.21 | ▲ +2.83% | ▲ +2.11% | $5.72 (+22.91%) |
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May 12, 2026
28d ago
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8-K
| $7.49 $7.03 | ▼ −6.14% | ▼ −4.98% | $5.72 (−23.63%) |
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Apr 17, 2026
7w ago
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DEFA14A
| $7.37 $7.03 | ▼ −4.61% | ▼ −5.53% | $5.72 (−22.39%) |
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Apr 3, 2026
9w ago
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S-3
| $6.90 $7.38 | ▲ +6.96% | ▲ +2.82% | $5.72 (−17.10%) |
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Mar 19, 2026
11w ago
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Press Release
| $6.07 $6.43 | ▲ +5.93% | ▲ +8.08% | $5.72 (−5.77%) |
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Mar 12, 2026
12w ago
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Press Release
| $6.15 $6.25 | ▲ +1.63% | ▲ +2.60% | $5.72 (−6.99%) |
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Mar 9, 2026
13w ago
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Press Release
| $7.17 $6.18 | ▼ −13.81% | ▼ −12.45% | $5.72 (−20.22%) |
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