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Relmada Therapeutics Provides Corporate Update and Reports Third Quarter 2023 Financial Results

November 08, 2023 | Last Trade: US$0.29 0.02 -5.19

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 8th 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
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Media Inquiries:

Corporate Communications
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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

 
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