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WKN: A2PSZF | ISIN: US75955J4022 | Ticker-Symbol: 4E2
Frankfurt
01.11.24
08:01 Uhr
2,900 Euro
-0,040
-1,36 %
Branche
Biotechnologie
Aktienmarkt
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1-Jahres-Chart
RELMADA THERAPEUTICS INC Chart 1 Jahr
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RELMADA THERAPEUTICS INC 5-Tage-Chart
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3,1403,28013:05
3,1603,32001.11.
PR Newswire
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Relmada Therapeutics, Inc.: Relmada Therapeutics Provides Corporate Update and Reports Third Quarter 2023 Financial Results

CORAL GABLES, Fla., Nov. 8, 2023 /PRNewswire/ -- Relmada Therapeutics, Inc. (Nasdaq: RLMD), a late-stage biotechnology company addressing diseases of the central nervous system (CNS), today provided a corporate update and announced preliminary and unaudited financial results for the third quarter ended September 30, 2023 . The Company will host a conference call today, Wednesday, November 8, at 4:30 PM Eastern Time/ 1:30 PM Pacific Time .

"We continue to advance our Phase 3 clinical development plan for REL-1017 as an adjunctive treatment for major depressive disorder (MDD)," said Sergio Traversa, Relmada's Chief Executive Officer. "Enrollment in the ongoing Reliance II (study 302) is progressing as planned and it remains on track to be completed in the in the first half of 2024. The initial patients have been enrolled into Relight, the new Phase 3 study (study 304), and we continue to anticipate the completion of this trial in the second half of next year. Additionally, we are encouraged by the recently announced efficacy and safety data from the one year, open-label safety study, Reliance-OLS (study 310), which showed rapid and sustained improvement in MADRS score with REL-1017 in both de novo patients and the full analysis set."

"We also recently presented new compelling preclinical data demonstrating the beneficial effect of non-psychedelic/low dose psilocybin on multiple metabolic parameters in a rodent model of metabolic dysfunction-associated steatotic liver disease (MASLD)," continued Mr. Traversa. "Based on these promising results, we intend to commence a single-ascending dose Phase 1 trial in obese patients with steatotic liver disease in early 2024 to define the pharmacokinetic, safety, and tolerability profile of our modified-release psilocybin formulation in this population, followed by a Phase 2a trial in the same patient population to establish clinical proof-of-concept. Importantly, there are currently no approved drugs for MASLD, and these initial pre-clinical data support the therapeutic potential of non-psychedelic/low dose psilocybin."

Recent Corporate Highlights

  • Enrollment is ongoing in Reliance II (study 302) and Relight (study 304), two sister pivotal Phase 3 trials of REL-1017 for the adjunctive treatment of MDD.

  • Announced results from recently completed Reliance-OLS (study 310), a long-term, open-label study of REL-1017 in MDD.

  • Rapid and sustained improvements in MADRS score were observed with REL-1017 in both de novo patient and the full analysis sets.

  • Announced new preclinical data from novel modified-release psilocybin program to be presented at the American Association for the Study of Liver Diseases (AASLD) The Liver Meeting® 2023.

    • Data demonstrated the beneficial effect of non-psychedelic/low dose psilocybin on multiple metabolic parameters in a rodent model of metabolic dysfunction-associated steatotic liver disease (MASLD).

  • Data presented from REL-1017 and psilocybin programs at the 36th European College of Neuropsychopharmacology (ECNP) Congress.

Upcoming Anticipated Milestones

  • Commence a Phase 1 trial in obese patients with steatotic liver disease in early 2024 to define the pharmacokinetic, safety and tolerability profile of the Company's modified-release psilocybin formulation, followed by a Phase 2a trial to establish clinical proof-of-concept.

  • Complete enrollment of Reliance II, which is planned to enroll approximately 300 patients, in the first half of 2024.

  • Complete enrollment of Relight (study 304), which is planned to enroll approximately 300 patients, in the second half of 2024.

Third Quarter 2023 Financial Results

  • Research and development expense for the three months ended September 30, 2023, totaled $10.5 million, compared to $30.5 million for the three months ended September 30, 2022 . The decrease was primarily associated with the completion of the Reliance I and Reliance III clinical studies in late 2022.

  • General and administrative expense for the three months ended September 30, 2023, totaled $12.2 million, compared to $8.2 million for the three months ended September 30, 2022 . The increase was primarily driven by an increase in stock-based compensation.

  • Net cash used in operating activities for the three months ended September 30, 2023 totaled $11.6 million, compared to $26.9 million for the three months ended September 30, 2022 .

  • Net loss for the three months ended September 30, 2023, was $22.0 million, or $0.73 per basic and diluted share, compared with a net loss of $39.4 million, or $1.31 per basic and diluted share, for the three months ended September 30, 2022 .

Nine Months Ended September 30, 2023 Financial Results

  • Research and development expense for the nine months ended September 30, 2023, totaled $40.1 million, compared to $86.5 million for the nine months ended September 30, 2022 . The decrease was primarily driven by a decrease in a study costs associated with the completion of Reliance I and III in late 2022.

  • General and administrative expense for the nine months ended September 30, 2023, totaled $36.8 million, compared to $36.1 million for the nine months ended September 30, 2022 . The increase was primarily driven by an increase in stock-based compensation.

  • Net cash used in operating activities for the nine months ended September 30, 2023 totaled $41.4 million, compared to $67.9 million for the three months ended September 30, 2022 .

  • Net loss for the nine months ended September 30, 2023 and 2022 was $73.6 million and $119.1 million, respectively. The Company had a net loss of $2.45 and $4.04 per share for the nine months ended September 30, 2023 and 2022, respectively.

  • As of September 30, 2023, the Company had cash, cash equivalents, and short-term investments of approximately $106.3 million, compared to cash, cash equivalents, and short-term investments of approximately $148.3 million at December 31, 2022 .

Conference Call and Webcast Details

Wednesday, November 8 th at 4:30 PM ET

Toll Free:

888-886-7786

International:

416-764-8658

Conference ID:

54664628

Webcast:

https://viavid.webcasts.com/starthere.jsp?ei=1636783&tp_key=a6209aa189

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 adjunctive treatment of major depressive disorder (MDD). The ongoing clinical research program is designed to evaluate the potential for REL-1017 as a rapid-acting, oral, once-daily antidepressant treatment.

About Relmada Therapeutics, Inc.

Relmada Therapeutics is a late-stage biotechnology company addressing diseases of the central nervous system (CNS), with a 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 is in late-stage development as an adjunctive treatment for MDD in adults. Relmada is also developing a novel non-psychedelic/low dose psilocybin for the treatment of metabolic indications. 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 potential failure of clinical trial results to demonstrate 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 the 310 open-label study to accurately reflect the results of the ongoing 302 and 304 blinded, randomized and controlled studies, failure to obtain regulatory approval of REL-1017 for the treatment of major depressive disorder, failure of the psilocybin program to advance to later stages of development, 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 should not be a complete list.

Investor Contact:

Tim McCarthy
LifeSci Advisors
[email protected]

Media Inquiries:

Corporate Communications
[email protected]

Relmada Therapeutics, Inc.

Condensed Consolidated Balance Sheets




As of







September 30,



As of




2023
(Unaudited)



December 31,
2022


Assets







Current assets:







Cash and cash equivalents


$

6,698,599



$

5,395,905


Short-term investments



99,568,502




142,926,781


Other receivables



-




512,432


Prepaid expenses



2,834,037




4,035,186


Total current assets



109,101,138




152,870,304


Other assets



47,715




34,875


Total assets


$

109,148,853



$

152,905,179











Commitments and Contingencies (See Note 6)


















Liabilities and Stockholders' Equity









Current liabilities:









Accounts payable


$

2,856,752



$

5,261,936


Accrued expenses



5,565,466




7,206,941


Total current liabilities



8,422,218




12,468,877











Stockholders' Equity:









Class A convertible preferred stock, $0.001 par value, 3,500,000 shares
authorized, none issued and outstanding



-




-


Common stock, $0.001 par value, 150,000,000 shares authorized, 30,099,203
shares issued and outstanding



30,099




30,099


Additional paid-in capital



636,434,059




602,517,138


Accumulated deficit



(535,737,523)




(462,110,935)


Total stockholders' equity



100,726,635




140,436,302


Total liabilities and stockholders' equity


$

109,148,853



$

152,905,179


Relmada Therapeutics, Inc.

Condensed Consolidated Statements of Operations

(Unaudited)




Three months ended



Nine months ended




September 30,



September 30,




2023



2022



2023



2022


Operating expenses:













Research and development


$

10,454,072



$

30,529,108



$

40,055,287



$

86,454,632


General and administrative



12,238,566




8,208,053




36,817,686




36,092,024


Total operating expenses



22,692,638




38,737,161




76,872,973




122,546,656



















Loss from operations



(22,692,638)




(38,737,161)




(76,872,973)




(122,546,656)



















Other (expenses) income:

















Gain on settlement of fees



-




-




-




6,351,606


Interest/investment income, net



1,321,441




827,614




3,892,478




1,544,898


Realized loss on short-term investments



(51,714)




(561,648)




(718,422)




(552,171)


Unrealized (loss) gain on short-term investments



(579,147)




(947,512)




72,329




(3,897,135)



















Total other (expense) income - net



690,580




(681,546)




3,246,385




3,447,198



















Net loss


$

(22,002,058)



$

(39,418,707)



$

(73,626,588)



$

(119,099,458)



















Loss per common share - basic and diluted


$

(0.73)



$

(1.31)



$

(2.45)



$

(4.04)



















Weighted average number of common shares
outstanding - basic and diluted



30,099,203




30,063,735




30,099,203




29,470,198


Relmada Therapeutics, Inc.

Condensed Consolidated Statements of Stockholders' Equity

(Unaudited)




Nine months ended September 30, 2023




Common Stock



Additional
Paid-in



Accumulated







Shares



Par Value



Capital



Deficit



Total


Balance - December 31, 2022



30,099,203



$

30,099



$

602,517,138



$

(462,110,935)



$

140,436,302


Stock-based compensation



-




-




11,354,466




-




11,354,466


Net loss



-




-




-




(26,321,576)




(26,321,576)


Balance - March 31, 2023



30,099,203




30,099




613,871,604




(488,432,511)




125,469,192


Stock-based compensation



-




-




11,169,517




-




11,169,517


Net loss



-




-




-




(25,302,954)




(25,302,954)


Balance - June 30, 2023



30,099,203



$

30,099



$

625,041,121



$

(513,735,465)



$

111,335,755


Stock-based compensation



-




-




11,392,938




-




11,392,938


Net loss



-




-




-




(22,002,058)




(22,002,058)


Balance - September 30, 2023



30,099,203




30,099




636,434,059




(535,737,523)




100,726,635





Nine months ended September 30, 2022




Common Stock



Additional
Paid-in



Accumulated







Shares



Par Value



Capital



Deficit



Total


Balance - December 31, 2021



27,740,147



$

27,740



$

513,304,258



$

(305,067,112)



$

208,264,886


Stock-based compensation



-




-




11,930,681




-




11,930,681


ATM offering, net



1,609,343




1,610




29,581,932




-




29,583,542


Warrant exercised for cash



33,334




33




299,973




-




300,006


Options exercised for cash



20,000




20




64,780




-




64,800


Net loss



-




-




-




(39,745,783)




(39,745,783)


Balance - March 31, 2022



29,402,824




29,403




555,181,624




(344,812,895)




210,398,132


Stock-based compensation



-




-




12,295,016




-




12,295,016


Warrant exercised for cash



91,058




91




595,259




-




595,350


Options exercised for cash



45,812




46




352,698




-




352,744


ATM offering, net of offering costs



484,900




485




13,144,572




-




13,145,057


Net loss



-




-




-




(39,934,968)




(39,934,968)


Balance - June 30, 2022



30,024,594




30,025




581,569,169




(384,747,863)




196,851,331


Stock-based compensation



-




-




8,343,139




-




8,343,139


Warrant exercised for cash



51,527




51




332,865




-




332,916


Options exercised for cash



17,886




18




286,158




-




286,176


Share exchange - Pre-funded warrants, net
of fees



(1,452,016)




(1,452)




(48,548)




-




(50,000)


Net loss



-




-




-




(39,418,707)




(39,418,707)


Balance - September 30, 2022



28,641,991



$

28,642



$

590,482,783



$

(424,166,570)



$

166,344,855


Relmada Therapeutics, Inc.

Condensed Consolidated Statements of Cash Flows

(Unaudited)




Nine months ended




September 30,




2023



2022


Cash flows from operating activities







Net loss


$

(73,626,588)



$

(119,099,458)


Adjustments to reconcile net loss to net cash used in operating activities:









Stock-based compensation



33,916,921




32,568,836


Realized loss on short-term investments



718,422




552,171


Unrealized (gain) loss on short-term investments



(72,329)




3,897,135


Change in operating assets and liabilities:









Lease payment receivable



-




86,377


Other receivable



512,432




-


Prepaid expenses and other assets



1,188,309




8,359,994


Accounts payable



(2,405,184)




(766,661)


Accrued expenses



(1,641,475)




6,482,889


Net cash used in operating activities



(41,409,492)




(67,918,717)











Cash flows from investing activities









Purchase of short-term investments



(57,151,963)




(38,993,173)


Sale of short-term investments



99,864,149




60,382,229


Net cash provided by investing activities



42,712,186




21,389,056











Cash flows from financing activities









Payment of fees for warrants issued for common stock



-




(50,000)


Proceeds from issuance of common stock - net



-




42,728,599


Proceeds from options exercised for common stock



-




703,720


Proceeds from warrants exercised for common stock



-




1,228,272


Net cash provided by financing activities



-




44,610,591











Net increase /(decrease) in cash and cash equivalents



1,302,694




(1,919,070)


Cash and cash equivalents at beginning of the period



5,395,905




44,443,439


Cash and cash equivalents at end of the period


$

6,698,599




42,524,369











Supplemental disclosure of cash flow information:


















Non-cash investing and financing activities:









Share exchange for Pre-funded warrants


$

-



$

1,452


SOURCE Relmada Therapeutics, Inc.

© 2023 PR Newswire
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