Earnings Call Summary | Relmada Therapeutics(RLMD.US) Q1 2024 Earnings Conference
Earnings Call Summary | Relmada Therapeutics(RLMD.US) Q1 2024 Earnings Conference
The following is a summary of the Relmada Therapeutics, Inc. (RLMD) Q1 2024 Earnings Call Transcript:
以下是Relmada Therapeutics, Inc.(RLMD)2024年第一季度業績電話會議記錄摘要:
Financial Performance:
財務業績:
Relmada Therapeutics reported a decrease in total research and development expenses to approximately $13.3 million in Q1 2024 from $15.9 million in Q1 2023.
General and administrative expenses also saw a decrease to $9.7 million in Q1 2024 from the previous year's $12.3 million.
The net loss for Q1 2024 was $21.8 million, lower than the $26.3 million reported for the same period in 2023.
As of March 31, 2024, the company had cash, cash equivalents, and short-term investments of approximately $83.6 million, compared to $96.3 million on December 31, 2023.
Relmada Therapeutics報告稱,研發總支出從2023年第一季度的1,590萬美元減少至2024年第一季度的約1,330萬美元。
一般和管理費用也從上一年的1,230萬美元減少到2024年第一季度的970萬美元。
2024年第一季度的淨虧損爲2180萬美元,低於2023年同期公佈的2630萬美元。
截至2024年3月31日,該公司的現金、現金等價物和短期投資約爲8,360萬美元,而2023年12月31日爲9,630萬美元。
Business Progress:
業務進展:
Progress continues with the ongoing Phase 3 program for REL-1017 in major depressive disorder (MDD), with improvements made to control the placebo response and improve patient profiles.
The company aims to strengthen the enrollment process by ensuring all qualifying criteria are met by patients.
A Phase 1 trial for obese patients following beneficial preclinical results on metabolic parameters in a rodent model of metabolic dysfunction is expected to begin in 2024.
Over the next 12 to 18 months, completion of the Reliance II study is anticipated, with the initiation of a Phase I clinical trial for their psilocybin formulation.
Improvements to clinical trial protocols, such as the requirement for detailed medical and pharmacy records, have been implemented to improve patient risk profiles.
The company is optimistic about the potential of their novel psilocybin derivative program, with additional progress reports expected later in 2024.
正在進行的重度抑鬱症 (MDD) REL-1017 三期計劃繼續取得進展,在控制安慰劑反應和改善患者概況方面做出了改進。
該公司旨在通過確保患者滿足所有資格標準來加強註冊流程。
一項針對肥胖患者的1期試驗預計將於2024年開始,該試驗將在齧齒類動物代謝功能障礙模型中的代謝參數上取得有益的臨床前結果。
在接下來的12至18個月中,預計Reliance II的研究將完成,其迷幻藥製劑的I期臨床試驗將啓動。
已經對臨床試驗協議進行了改進,例如要求提供詳細的醫療和藥房記錄,以改善患者的風險狀況。
該公司對其新型迷幻藥衍生物計劃的潛力持樂觀態度,預計將在2024年晚些時候發佈更多進展報告。
More details: Relmada Therapeutics IR
更多詳情: Relmada 治療公司 IR
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譯文內容由第三人軟體翻譯。