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Relmada Therapeutics to Participate in the Goldman Sachs 43rd Annual Global Healthcare Conference

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Relmada Therapeutics (NASDAQ: RLMD), a late-stage biotechnology firm focused on central nervous system diseases, announced that CEO Sergio Traversa will participate in the Goldman Sachs 43rd Annual Global Healthcare Conference on June 14, 2022, at 10:40am PT / 1:40pm ET. The event will discuss the company's lead program, REL-1017, a new chemical entity in late-stage development for major depressive disorder (MDD). A webcast of the presentation will be available, with an archived replay accessible for 90 days.

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CORAL GABLES, Fla., June 7, 2022 /PRNewswire/ -- Relmada Therapeutics, Inc. (NASDAQ: RLMD), a late-stage biotechnology company addressing diseases of the central nervous system (CNS), today announced that Sergio Traversa, Chief Executive Officer, will participate in a fireside chat at the Goldman Sachs 43rd Annual Global Healthcare Conference on Tuesday, June 14, 2022, at 10:40am PT / 1:40pm ET. Please find additional details about the event below.

Goldman Sachs 43rd Annual Global Healthcare Conference
Date: Tuesday, June 14, 2022, 10:40-11:15am PT / 1:40-2:15pm ET
Webcast: https://kvgo.com/gs/relmada-therapeutics-inc-june-2022

The webcast can also be accessed in the Investors section of the Relmada website at https://www.relmada.com/investors/ir-calendar. An archived replay will be available for 90 days after the conclusion of the event.

About REL-1017

REL-1017, a new chemical entity (NCE) and novel NMDA receptor (NMDAR) channel blocker that preferentially targets hyperactive channels while maintaining physiological glutamatergic neurotransmission, is currently in late-stage development for the treatment of major depressive disorder (MDD). The ongoing Reliance Clinical Research Program is designed to evaluate the potential for REL-1017 as a rapid-acting, oral, once-daily antidepressant treatment. In a Phase 2 trial, REL-1017 demonstrated rapid, robust, and sustained antidepressant effects with statistically significant improvements compared to placebo. The Phase 2 study also showed a favorable pharmacokinetic, safety, and tolerability profile of REL-1017 consistent with results observed in previously completed Phase 1 studies.

About Relmada Therapeutics, Inc.

Relmada Therapeutics is a late-stage biotechnology company addressing diseases of the central nervous system (CNS), with focus on major depressive disorder (MDD). Relmada's experienced and dedicated team is committed to making a difference in the lives of patients and their families. Relmada's lead program, REL-1017, is a new chemical entity (NCE) and novel NMDA receptor (NMDAR) channel blocker that preferentially targets hyperactive channels while maintaining physiological glutamatergic neurotransmission. REL-1017 has entered late-stage development as an adjunctive and monotherapy treatment for MDD. In addition, Relmada is advancing a clinical-stage program in neurodegenerative diseases based on psilocybin and select derivative molecules. Learn more at 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 "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 the 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 should not be a complete list.

Investor Contact:
Tim McCarthy
LifeSci Advisors
212-915-2564
tim@lifesciadvisors.com 

Media Inquiries:
FischTank PR
relmada@fischtankpr.com 

Cision View original content to download multimedia:https://www.prnewswire.com/news-releases/relmada-therapeutics-to-participate-in-the-goldman-sachs-43rd-annual-global-healthcare-conference-301562802.html

SOURCE Relmada Therapeutics, Inc.

FAQ

What is the date of Relmada Therapeutics' participation in the Goldman Sachs Conference?

Relmada Therapeutics will participate in the Goldman Sachs 43rd Annual Global Healthcare Conference on June 14, 2022.

What time will Relmada's CEO speak at the Goldman Sachs Healthcare Conference?

Sergio Traversa, CEO of Relmada Therapeutics, will speak at 10:40am PT / 1:40pm ET.

How can I access the webcast of Relmada Therapeutics' conference presentation?

The webcast can be accessed at https://kvgo.com/gs/relmada-therapeutics-inc-june-2022 and will be available for replays for 90 days.

What is REL-1017 and its relevance to Relmada Therapeutics?

REL-1017 is Relmada's lead program, currently in late-stage development for treating major depressive disorder.

What are the results of the Phase 2 trial for REL-1017?

The Phase 2 trial of REL-1017 demonstrated rapid and sustained antidepressant effects compared to placebo.

Relmada Therapeutics, Inc.

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