Relmada Therapeutics Provides Regulatory Update Confirming FDA Alignment on Registrational Studies Design for NDV-01 for Two Separate Indications
MWN-AI** Summary
On January 12, 2026, Relmada Therapeutics, Inc. announced a significant regulatory update regarding its lead candidate NDV-01 for treating non-muscle invasive bladder cancer (NMIBC). The U.S. Food and Drug Administration (FDA) provided written feedback that aligns with Relmada’s proposed clinical trial designs for two distinct patient populations, signaling progress toward potential new therapies in an unmet medical need.
The FDA endorsed a single-arm, open-label Phase 3 trial for NDV-01 in patients with 2nd-line refractory high-grade NMIBC with carcinoma in situ (CIS), a particularly difficult-to-treat group. This study is designed to evaluate the complete response (CR) rate and duration of response (DOR). The FDA also supported a randomized trial comparing NDV-01 to observation in the adjuvant setting for intermediate-risk NMIBC, aiming to assess disease-free survival (DFS). Both trials are set to commence in the first half of 2026, reflecting the FDA's commitment to expediting treatment options for these patient categories.
Dr. Raj S. Pruthi, Chief Medical Officer of Oncology at Relmada, expressed satisfaction with the FDA’s recommendations, emphasizing the importance of a bladder-sparing therapeutic approach for patients who lack effective alternatives. NDV-01 is a sustained-release formulation combining gemcitabine and docetaxel, designed for easy administration in less than five minutes without the need for anesthesia.
Given that NMIBC accounts for 75-80% of bladder cancer cases and presents high recurrence rates, NDV-01 could potentially revolutionize treatment paradigms for this population, aiming to provide both frontline and salvage therapy options. As Relmada prepares for its upcoming clinical studies, the focus remains on addressing considerable unmet needs in bladder cancer treatment.
MWN-AI** Analysis
Relmada Therapeutics, Inc. (Nasdaq: RLMD) recently reported a significant regulatory milestone with the FDA, confirming an aligned pathway for their investigational drug, NDV-01, in treating two critical forms of non-muscle invasive bladder cancer (NMIBC). This news is essential for investors considering entry or expansion in biotech portfolios focused on oncology.
The FDA’s feedback indicates a green light for Relmada’s proposed registrational studies. The first study targets 2nd-line refractory high-grade NMIBC with carcinoma in situ (CIS) using a single-arm, open-label design, and the second study focuses on intermediate-risk NMIBC in an adjuvant setting, comparing NDV-01 to observation via a randomized trial. Given the lack of approved therapies in these segments, this alignment not only streamlines the regulatory approach but also highlights the unmet medical need in these patient populations.
From a market perspective, this development significantly enhances NDV-01’s potential value. With NMIBC accounting for 75-80% of all bladder cancer cases and a notable high recurrence rate (50-80% over five years), the therapeutic market is ripe for innovative solutions. Furthermore, NDV-01’s formulation allows for in-office administration without anesthesia, enhancing patient compliance and marketability.
Looking ahead, both registrational trials are anticipated to initiate in the first half of 2026. Investors should monitor upcoming Phase 2 results as they could influence clinical and market advancements. The potential for NDV-01 to be positioned as a frontline or salvage therapy across multiple NMIBC subtypes adds to its attractiveness.
In summary, Relmada's progress not only supports a strong case for NDV-01 but also positions the company favorably within the oncology biotech space. Investors should consider this development as a positive indicator of growth potential, keeping an eye on trial progress and broader market receptions.
**MWN-AI Summary and Analysis is based on asking OpenAI to summarize and analyze this news release.
FDA written feedback supports:
- a single-arm, open-label registrational trial in 2nd-line refractory high-grade NMIBC with CIS
- a randomized vs observation single trial in intermediate-risk NMIBC in the adjuvant setting
Phase 3 program expected to initiate in 1H 2026
CORAL GABLES, Fla., Jan. 12, 2026 (GLOBE NEWSWIRE) -- Relmada Therapeutics, Inc. (Nasdaq: RLMD, “Relmada” or the “Company”), a clinical-stage biotechnology company advancing innovative therapies for oncology and central nervous system disorders, today announced that it has received written feedback from the U.S. Food and Drug Administration (FDA) regarding the registrational development pathway for NDV-01 in 2nd-line refractory, high-grade BCG-unresponsive non-muscle invasive bladder cancer (NMIBC) with carcinoma in situ (CIS) -- one of the highest-risk and most treatment-resistant NMIBC populations -- and in intermediate risk NMIBC in the adjuvant setting, where there are currently no approved therapies.
In its written response to Relmada’s Type B pre-IND submission, the FDA indicated that a single-arm, open-label clinical trial in this high-grade, BCG-unresponsive with CIS population is an appropriate registrational approach for NDV-01. This feedback provides a clear and efficient development path toward a potential NDA submission for NDV-01 as a bladder-sparing therapeutic option in a patient population with significant unmet need.
The FDA also provided separate, supportive written feedback on the Company’s planned single registrational study in intermediate-risk NMIBC in the adjuvant setting, which is expected to follow an open-label, randomized-to-observation design.
Relmada continues to anticipate initiating both registrational trials in the first half of 2026.
“We are very pleased with the FDA’s alignment on the registrational design for NDV-01 in high-grade BCG-unresponsive NMIBC,” said Raj S. Pruthi, MD, Chief Medical Officer – Oncology at Relmada Therapeutics. “A single-arm pivotal study in this setting represents a meaningful opportunity to advance an in-office, bladder-sparing therapy for patients who have few if any effective alternatives. This study represents the fastest path to approval for NDV-01.”
Dr. Pruthi continued, “We are also encouraged by the FDA’s feedback on our intermediate-risk registration plans, where we believe NDV-01 could potentially provide meaningful clinical benefit to patients where no approved treatments currently exist.”
About the Planned High-Grade Registrational Study
The planned pivotal Phase 3 study in 2nd-line, refractory, high-grade BCG-unresponsive NMIBC with carcinoma in situ (CIS) will be an open-label, single-arm trial evaluating:
- Primary endpoint: Complete response (CR) rate at any time
- Key secondary endpoint: Duration of response (DOR)
- Assessments: Cystoscopy, cytology, and biopsy per protocol
The design reflects FDA’s written guidance on the study population, endpoint selection, and evaluation methodology and is consistent with prior FDA precedents for single-arm registrational trials in NMIBC.
About the Planned Intermediate-Risk Registrational Study
The planned pivotal Phase 3 study in intermediate-risk NMIBC in the adjuvant setting will be an open label randomized-to-observation study:
- Primary endpoint: Disease Free Survival (DFS)
- Key secondary endpoint: Duration of response (DOR)
- Assessments: Cystoscopy, cytology, and biopsy per protocol
The design reflects FDA’s written guidance on the study population, endpoint selection, and evaluation methodology.
About NDV-01
NDV-01 is a sustained-release, intravesical formulation of gemcitabine and docetaxel (Gem/Doce), in development for the treatment of non-muscle invasive bladder cancer. It is designed to enable Gem/Doce bladder retention and gradual drug release over ten days. The formulation creates a soft matrix that enhances local exposure while minimizing systemic toxicity. The NDV-01 formulation is a ready to use, convenient to administer in-office in less than five minutes, and does not require anesthesia or specialized equipment. It is protected by patents through 2038.
About NMIBC
NMIBC represents 75-80% of all bladder cancer cases and is associated with high recurrence (50 – 80% over 5 years). With over 744,000 prevalent cases in the U.S. and limited treatment options, the market opportunity is significant. High-grade BCG-unresponsive disease represents one of the most difficult-to-treat NMIBC subtypes, with limited bladder-sparing options. Intermediate-risk NMIBC in the adjuvant setting has no currently approved therapies. NDV-01 has the potential to serve as a frontline or salvage therapy and could be applicable across multiple NMIBC subtypes.
About Relmada Therapeutics, Inc.
Relmada Therapeutics is a clinical-stage biotechnology company focused on developing transformative therapies for oncology and central nervous system conditions. Its lead candidates, NDV-01 and sepranolone, are advancing through mid-stage clinical development with the potential to address significant unmet needs.
For more information, visit www.relmada.com
Forward-Looking Statements:
The Private Securities Litigation Reform Act of 1995 provides a safe harbor for forward-looking statements made by us or on our behalf. This press release contains statements which constitute “forward-looking statements” within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. Any statement that is not historical in nature is a forward-looking statement and may be identified by the use of words and phrases such as “if”, “may”, “expects”, “anticipates”, “believes”, “will”, “will likely result”, “will continue”, “plans to”, “potential”, “promising”, and similar expressions. These statements are based on management’s current expectations and beliefs and are subject to a number of risks, uncertainties and assumptions that could cause actual results to differ materially from those described in the forward-looking statements, including potential for Relmada’s product candidates to progress, including the potential for Phase 2 NDV-01 data to continue to deliver positive results supporting further development, potential for clinical trials to deliver statistically and/or clinically significant evidence of efficacy and/or safety, failure of top-line results to accurately reflect the complete results of the trial, failure of planned or ongoing preclinical and clinical studies to demonstrate expected results, potential failure to continue to secure FDA agreement on the regulatory path for NDV-01 and/or sepranolone, or that future NDV-01 and/or sepranolone clinical results will be acceptable to the FDA, failure to secure adequate NDV-01 and/or sepranolone drug supply, the Company’s cash runway and sufficiency of the Company’s cash resources and uncertainties inherent in estimating the Company’s cash runway, future expenses and other financial results, including its ability to fund future operations, including clinical trials, and the other risk factors described under the heading “Risk Factors” set forth in the Company’s reports filed with the SEC from time to time. No forward-looking statement can be guaranteed, and actual results may differ materially from those projected. Relmada undertakes no obligation to publicly update any forward-looking statement, whether as a result of new information, future events, or otherwise. Readers are cautioned that it is not possible to predict or identify all the risks, uncertainties and other factors that may affect future results and that the risks described herein are not a complete list.
Investor Contact:
Brian Ritchie
LifeSci Advisors
britchie@lifesciadvisors.com
Media Inquiries:
Corporate Communications
media@relmada.com
FAQ**
How does the FDA's feedback on the single-arm trial design for Relmada Therapeutics Inc. (RLMD) in high-grade BCG-unresponsive NMIBC align with previous precedents for similar trials in this indication?
What specific concerns, if any, did the FDA raise regarding the randomized vs. observation trial design for intermediate-risk NMIBC, as proposed by Relmada Therapeutics Inc. (RLMD)?
Given the significant unmet need in the NMIBC population, how does Relmada Therapeutics Inc. (RLMD) plan to approach potential partner collaborations or funding opportunities for the development of NDV-01?
In light of the FDA's supportive feedback, what key milestones does Relmada Therapeutics Inc. (RLMD) aim to achieve ahead of the expected initiation of both registrational trials in H1 2026?
**MWN-AI FAQ is based on asking OpenAI questions about Relmada Therapeutics Inc. (NASDAQ: RLMD).
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