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Forte Biosciences, Inc. Announces First Quarter 2024 Results and Provides Business Update

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Forte Biosciences, a clinical-stage biopharmaceutical firm, announced its Q1 2024 results. The company reported a net loss of $7.4 million, or $0.16 per share, an improvement from $0.32 per share in the same period last year. Forte's cash reserves stood at $30.4 million by the end of the quarter. R&D expenses dropped to $4.4 million from $4.8 million YoY, while G&A expenses rose to $3.5 million from $2.1 million. The company's phase 1 trial for its drug candidate FB102 has shown a good safety profile, with completion of multiple ascending dose cohorts expected mid-year. Forte plans to start patient-based studies by year-end, aiming to address various autoimmune diseases.

Positive
  • Net loss per share improved from $0.32 to $0.16 YoY.
  • R&D expenses decreased from $4.8 million to $4.4 million YoY.
  • FB102 phase 1 trial showed a good safety profile.
  • Completion of multiple ascending dose cohorts expected mid-year.
  • Plans to initiate patient-based studies by year-end.
Negative
  • Net loss increased to $7.4 million from $6.7 million YoY.
  • Cash and cash equivalents decreased from $37.1 million to $30.4 million.
  • G&A expenses rose significantly from $2.1 million to $3.5 million YoY.
  • Total assets decreased from $39 million to $32 million YoY.

Insights

Forte Biosciences reported a net loss of $7.4 million for the first quarter of 2024, which is an increase from the $6.8 million loss in the same period last year. The company’s research and development (R&D) expenses decreased slightly to $4.4 million, down from $4.8 million. This reduction is mainly due to lower manufacturing costs, though it was partially offset by higher clinical and payroll expenses.

On the other hand, general and administrative (G&A) expenses jumped to $3.5 million from $2.1 million in the previous year, driven by increased legal and professional fees. This rise in G&A expenses could be a concern as it reflects higher overhead costs that may not directly contribute to the advancement of their clinical programs.

Forte completed the quarter with $30.4 million in cash and cash equivalents, down from $37.1 million at the end of 2023. This cash position is important for funding their ongoing clinical trials and operations. Retail investors should monitor the company’s cash burn rate and upcoming financing needs, as this could impact future share dilution.

Net losses per share improved to ($0.16) from ($0.32), largely due to an increase in the number of shares outstanding.

Forte Biosciences' advancements with their lead candidate FB102 are noteworthy. The company has completed the single ascending dose (SAD) portion of their Phase 1 trial and is progressing into the multiple ascending dose (MAD) cohorts. The early data showing a good safety profile is promising, especially for a drug targeting autoimmune and autoimmune-related diseases. Safety in early trials is a critical milestone, as it can significantly de-risk the program moving forward.

Initiating patient-based studies later this year will be a pivotal step. These studies will provide deeper insights into the drug's efficacy and potential market impact. The reference to large addressable markets suggests that FB102 could address significant unmet medical needs, which is a positive indicator for future revenue streams if clinical trials prove successful.

Investors should watch for upcoming data releases on the MAD cohorts and initial patient studies, as these will be important in validating the drug’s therapeutic potential and positioning within the competitive landscape of autoimmune disease treatments.

DALLAS--(BUSINESS WIRE)-- Forte Biosciences, Inc. (www.fortebiorx.com) (NASDAQ: FBRX), a clinical-stage biopharmaceutical company focused on autoimmune and autoimmune-related diseases, today announced first quarter 2024 results and provided a business update.

First Quarter 2024 Business Highlights

“Forte continues to make excellent progress with FB102. As we indicated last quarter, the single ascending dose (SAD) portion of the FB102 phase 1 trial was successfully completed. We expect the dosing of the multiple ascending dose (MAD) cohorts of the phase 1 trial in the healthy volunteers to complete around mid-year. To date, FB102 has demonstrated a good safety profile, including in the MAD cohorts,” said Paul Wagner, Ph.D., Chairman and Chief Executive Officer of Forte Biosciences. “We look forward to initiating patient-based studies before the end of the year. We believe the data to date supports the significant potential for FB102 across a variety of autoimmune and autoimmune-related diseases with large addressable markets and we look forward to addressing these opportunities as we continue to advance the FB102 program.”

First Quarter 2024 Operating Results

Research and development expenses were $4.4 million for the three months ended March 31, 2024, compared to $4.8 million for the same period in 2023. The decrease was primarily due to a decrease of approximately $2.7 million in manufacturing costs partially offset by an increase of approximately $1.4 million in clinical expenses as we advanced our FB102 program through clinical trials, and a net increase of approximately $0.9 million in payroll and related expenses due to an increase in our average headcount.

General and administrative expenses were $3.5 million for the three months ended March 31, 2024, compared to $2.1 million for the same period in 2023. The increase was primarily due to increases in legal and professional expenses.

Net losses per share were ($0.16) and ($0.32) for the three months ended March 31, 2024 and 2023, respectively.

Forte ended the first quarter 2024 with approximately $30.4 million in cash and cash equivalents. Forte had approximately 36.4 million shares of common stock outstanding as of March 31, 2024.

CONDENSED CONSOLIDATED BALANCE SHEETS

(in thousands except share and par value data)

 
March 31, 2024 December 31, 2023
(unaudited)
Assets
Current assets:
Cash and cash equivalents

$

30,444

 

$

37,125

 

Prepaid expenses and other current assets

 

1,058

 

 

1,202

 

Total current assets

 

31,502

 

 

38,327

 

 
Property and equipment, net

 

106

 

 

109

 

Other assets

 

409

 

 

544

 

Total assets

$

32,017

 

$

38,980

 

 
Liabilities and stockholders' equity
Current liabilities:
Accounts payable

$

1,685

 

$

1,424

 

Accrued liabilities

 

1,647

 

 

2,242

 

Total current liabilities

 

3,332

 

 

3,666

 

 
Commitments and contingencies (Note 6)
Stockholders’ equity
Common stock, $0.001 par value: 200,000,000 shares authorized as of March 31, 2024 (unaudited) and December 31, 2023; 36,394,882 and 36,335,105 shares issued and outstanding as of March 31, 2024 (unaudited) and December 31, 2023, respectively

 

36

 

 

36

 

Additional paid-in capital

 

154,591

 

 

153,794

 

Accumulated other comprehensive income (loss)

 

(2

)

 

4

 

Accumulated deficit

 

(125,940

)

 

(118,520

)

Total stockholders’ equity

 

28,685

 

 

35,314

 

Total liabilities and stockholders’ equity

$

32,017

 

$

38,980

 

CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS

(in thousands, except share and per share amounts)

 
For the Three Months Ended March 31,

 

2024

 

 

2023

 

Operating expenses:
Research and development (including $29 and $0 of related party transactions for the 3 months ending March 31, 2024 and 2023, respectively)

$

4,353

 

$

4,787

 

General and administrative

 

3,451

 

 

2,068

 

Total operating expenses

 

7,804

 

 

6,855

 

Loss from operations

 

(7,804

)

 

(6,855

)

Other income, net

 

384

 

 

102

 

Net loss

$

(7,420

)

$

(6,753

)

Per share information:
Net loss per share - basic and diluted

$

(0.16

)

$

(0.32

)

 
Weighted average shares and pre-funded warrants outstanding, basic and diluted

 

46,082,861

 

 

21,006,680

 

 
Comprehensive Loss:
Net loss

$

(7,420

)

$

(6,753

)

Unrealized loss on available-for-sale securities

 

(6

)

 

 

Comprehensive loss

$

(7,426

)

$

(6,753

)

Additional details on our first quarter 2024 financial results can be found in Forte’s Form 10-Q as filed with the SEC on May 13, 2024. You can also find more information in the investor relations section of our website at www.fortebiorx.com.

About Forte

Forte Biosciences, Inc. is a clinical-stage biopharmaceutical company that is advancing its product candidate, FB102, which is a proprietary molecule with potentially broad autoimmune and autoimmune-related applications including in such indications as graft-versus-host disease, vitiligo and alopecia areata.

Forward-Looking Statements

Forte cautions you that statements included in this press release that are not a description of historical facts are forward-looking statements. In some cases, you can identify forward-looking statements by terms such as “may,” “will,” “should,” “expect,” “plan,” “anticipate,” “could,” “intend,” “target,” “project,” “contemplates,” “believes,” “estimates,” “predicts,” “potential” or “continue” or the negatives of these terms or other similar expressions. These statements are based on the Company’s current beliefs and expectations. Forward-looking statements include statements regarding the Company’s beliefs, goals, intentions and expectations regarding its product candidate, FB102 and the therapeutic and commercial market potential of FB102. Actual results and the timing of events could differ materially from those anticipated in such forward-looking statements as a result of various risks and uncertainties, which include, without limitation: risks related to Forte’s ability to obtain sufficient additional capital to continue to advance Forte’s product candidate, FB102; uncertainties associated with the clinical development and regulatory approval of Forte’s product candidate, FB102, including potential delays in the commencement, enrollment and completion of clinical trials, including the timing of the commencement of the Company’s patient-based studies; the risk that results from preclinical and any interim result of our ongoing phase 1 clinical trials may not be predictive of future results from clinical trials; risks associated with the failure to realize any value from FB102 in light of inherent risks, expense and difficulties involved in successfully bringing product candidates to market; and additional risks, uncertainties, and other information affecting Forte’s business and operating results is contained in Forte’s Annual Report on Form 10-K for the year ended December 31, 2023, as filed with the Securities and Exchange Commission on March 18, 2024, in the Company’s subsequent Quarterly Report on Form 10-Q filed on May 13, 2024 and in its other filings with the Securities and Exchange Commission. All forward-looking statements in this press release are current only as of the date hereof and, except as required by applicable law, Forte undertakes no obligation to revise or update any forward-looking statement, or to make any other forward-looking statements, whether as a result of new information, future events or otherwise. All forward-looking statements are qualified in their entirety by this cautionary statement. This caution is made under the safe harbor provisions of the Private Securities Litigation Reform Act of 1995.

LifeSci Advisors

Mike Moyer, Managing Director

mmoyer@lifesciadvisors.com

Forte Biosciences, Inc.

Paul Wagner, CEO

investors@fortebiorx.com

Source: Forte Biosciences, Inc.

FAQ

What were Forte Biosciences' net losses in Q1 2024?

Forte Biosciences reported a net loss of $7.4 million in Q1 2024.

How much has Forte Biosciences' net loss per share improved in Q1 2024 compared to Q1 2023?

Forte Biosciences' net loss per share improved from $0.32 in Q1 2023 to $0.16 in Q1 2024.

What were Forte Biosciences' cash reserves at the end of Q1 2024?

Forte Biosciences had $30.4 million in cash and cash equivalents at the end of Q1 2024.

How did Forte Biosciences' R&D expenses change in Q1 2024?

Forte Biosciences' R&D expenses decreased to $4.4 million in Q1 2024 from $4.8 million in Q1 2023.

What was the increase in Forte Biosciences' G&A expenses in Q1 2024?

Forte Biosciences' G&A expenses increased from $2.1 million in Q1 2023 to $3.5 million in Q1 2024.

What is the status of Forte Biosciences' FB102 phase 1 trial?

The single ascending dose portion of FB102 phase 1 trial was successfully completed, and the multiple ascending dose cohorts are expected to be completed by mid-year.

When does Forte Biosciences plan to start patient-based studies for FB102?

Forte Biosciences plans to initiate patient-based studies for FB102 before the end of 2024.

Forte Biosciences, Inc.

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