RLMD stock touches 52-week low at $0.71 amid market fluctuations

Published 04/12/2024, 15:32
RLMD stock touches 52-week low at $0.71 amid market fluctuations
RLMD
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In a volatile trading session, Relmada Therapeutics Inc. (NASDAQ:RLMD) stock has plunged to its 52-week low, reaching a price level of just $0.71. With a market capitalization of $83.58 million, the company maintains strong liquidity with a current ratio of 6.89, indicating solid short-term financial stability. This significant downturn in the stock's performance marks a stark contrast to the overall 1-year change, which has seen the company's stock value increase by 10.8%. Investors are closely monitoring the stock as it navigates through challenging market conditions, with many keeping an eye on potential rebounds or further declines in the near future. According to InvestingPro analysis, the stock appears undervalued at current levels, with analyst price targets ranging from $2 to $23.Want deeper insights? InvestingPro subscribers have access to 7 additional key insights and a comprehensive Pro Research Report for RLMD, helping investors make more informed decisions.

In other recent news, Relmada Therapeutics, Inc. experienced a significant setback as its Phase 3 Reliance II study of REL-1017, intended for major depressive disorder (MDD), was deemed futile by the independent Data Monitoring Committee (DMC). Despite this, the company remains committed to the development of REL-P11, a candidate for treating metabolic disease, currently in a Phase 1 first-in-human study. Financially, as of September 30, 2024, Relmada reported a robust position with approximately $54.1 million in cash and cash equivalents.

Furthermore, Mizuho (NYSE:MFG) analyst Uy Ear expressed disappointment with the futility finding for REL-1017's study. In terms of financials, the company's Q3 report showed a decrease in cash and investments to $54.1 million and a net loss of $21.7 million. Research and development expenses have risen to $11.1 million, funding ongoing studies including a Phase 1 safety study for a psilocybin-based candidate and plans for a Phase 2a study in the upcoming year.

These are among the recent developments concerning Relmada Therapeutics, which despite the challenges, continues its research and development efforts, particularly with REL-1017. The company's forward-looking statements indicate management's expectations and projections, subject to various risks and uncertainties that could cause actual results to differ materially from those anticipated.

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