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Spruce Biosciences Reports Fourth Quarter and Full Year 2020 Financial Results and Provides Recent Corporate Updates

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Spruce Biosciences, Inc. (Nasdaq: SPRB) reported its Q4 and 2020 financial results, marking a transformative year in developing therapies for rare endocrine disorders.

Key updates include the initiation of the CAHmelia program for classic congenital adrenal hyperplasia and plans for Phase 2 trials in pediatric classic CAH and PCOS. The company has $157.2 million in cash, enhancing its ability to fund ongoing clinical studies. R&D expenses rose significantly to $23.9 million, with a net loss of $29.5 million reported for the year.

Positive
  • Initiation of CAHmelia program for adult classic CAH.
  • Well-capitalized with $157.2 million in cash to fund ongoing pipeline advancements.
  • Increased attention from institutional investors after being added to Russell indexes.
  • Patent issued for tildacerfont extending exclusivity through 2038.
Negative
  • Net loss of $29.5 million for 2020 compared to $13.1 million in 2019.
  • Significant increase in R&D expenses from $10.8 million in 2019 to $23.9 million in 2020, indicating higher cash burn.

Spruce Biosciences, Inc. (Nasdaq: SPRB), a late-stage biopharmaceutical company focused on developing and commercializing novel therapies for rare endocrine disorders with significant unmet medical need, today reported financial results for the fourth quarter and full year ended December 31, 2020 and provided a corporate update.

“2020 was a transformative year for Spruce Biosciences, as we firmly established our company as an emerging leader in the development of groundbreaking therapies for rare endocrine disorders,” said Richard King, Chief Executive Officer, Spruce Biosciences. “The initiation of our CAHmelia program in adult classic congenital adrenal hyperplasia (CAH) moves us one step closer to changing the treatment paradigm for patients living with this chronic and potentially life-threatening disease. Following the completion of our upsized IPO in October 2020, we are also preparing to expand the utility of tildacerfont through studies in children with classic CAH and in women living with a rare form of polycystic ovary syndrome (PCOS), with Phase 2 programs in both indications on track to initiate in the second half of 2021. We also remain focused on clinical study execution: we have the majority of our CAHmelia study sites now active across 2 continents and are encouraged by the level of patient interest registered with our study investigators and at CAHstudy.com.”

King continued, “Following discussions with U.S. Food and Drug Administration, we have decided to increase the open label extension period for CAHmelia-203 by 18 weeks and for CAHmelia-204 by 24 weeks. In addition, we have increased the size of CAHmelia-204 from 60 patients to 90 patients. We believe that these changes will result in a more robust data package. With these program enhancements, together with the impact of the ongoing COVID-19 pandemic, we now expect primary data from CAHmelia-203 in the first half of 2022 and CAHmelia-204 in the second half of 2022. Assuming positive study outcomes, we continue to target an NDA filing for tildacerfont in adult classic CAH in 2023.”

Recent Operating Highlights

  • Presentation of Phase 1 and 2 Data of Tildacerfont at Endocrine’s Society’s 2021 Annual Meeting (ENDO 2021): In March 2021, data from the company’s Phase 1 and 2 programs of tildacerfont in classic CAH were presented at ENDO 2021. The presentation highlighted several datasets, including data from the company’s SPR001-202 study, which demonstrated the ability of tildacerfont to reduce and normalize key disease biomarkers over a 12-week period. Normalization of highly elevated hormones in classic CAH patients over a 12-week study and without increases to daily steroid doses has not been reported to date with any other investigational product candidate.

  • Submission of Pediatric Investigation Plan (PIP) to the European Medicines Agency (EMA): Spruce has submitted a PIP to the Pediatric Committee of the EMA regarding a registrational program in pediatric classic CAH.

  • Patent Issuance Extends Tildacerfont Exclusivity Through 2038: In December 2020, the United States Patent and Trademark Office issued US Patent Number 10,849,908 titled “Corticotrophin releasing factor antagonists.” This newly issued patent covers broad claims regarding the use of a CRF1 receptor antagonist for the treatment of CAH, builds on existing composition of matter patents, and further extends exclusivity through 2038.

  • Addition to Russell 2000®, 3000®, and Microcap® Indexes: In December 2020, the company was added to the Russell 2000®, 3000®, and Microcap® indexes as part of Russell’s quarterly additions of selected initial public offering (IPOs). The additions increase overall awareness and visibility of the company within the investment community and may broaden its institutional shareholder base.

  • Amended Debt Facility with Silicon Valley Bank (SVB) Provides Access to $25 Million in Non-Dilutive Financing: The company has amended its debt facility with SVB to increase the aggregate principal amount of the term loan commitment by SVB from $4.5 million to $30 million. The amendment refinances and delays repayment of principal of the existing $4.5 million term loan to 2023 and provides access up to $25 million in additional non-dilutive financing for general corporate purposes.

  • Cash and Cash Equivalents of $157.2 Million at 2020 Year End: Following the IPO in October 2020, the company is well capitalized to advance its pipeline through major milestones, including primary data readout from its late-stage CAHmelia program and Phase 2 programs in pediatric classic CAH and a rare form of PCOS.

Anticipated Upcoming Milestones

  • Filing of an Investigational New Drug (IND) application in the first half of 2021 in PCOS
  • Initiation of a Phase 2 proof-of-concept clinical trial in the second half of 2021 in PCOS
  • Initiation of a Phase 2 clinical program in pediatric classic CAH in the second half of 2021

Financial Highlights

  • Cash and Cash Equivalents: Cash and cash equivalents as of December 31, 2020, were $157.2 million.

  • Research and Development (R&D) Expenses: R&D expenses for the fourth quarter and full year ended December 31, 2020 were $5.8 million and $23.9 million compared to $2.8 million and $10.8 million for the same periods in 2019, respectively. The overall increase in R&D expenses was primarily related to the advancement of tildacerfont into late-stage clinical development.

  • General and Administrative (G&A) Expenses: G&A expenses for the fourth quarter and full year ended December 31, 2020 were $2.5 million and $5.6 million, compared to $0.3 million and $2.3 million for the same periods in 2019, respectively. The overall increase in G&A expenses was primarily driven by an increase in costs related to operation as a public company.

  • Net Loss: Net loss for the fourth quarter and full year ended December 31, 2020 was $8.3 million and $29.5 million, compared to $3.2 million and $13.1 million for the same periods in 2019, respectively.

About Spruce Biosciences

Spruce Biosciences is a late-stage biopharmaceutical company focused on developing and commercializing novel therapies for rare endocrine disorders with significant unmet need. Spruce is initially developing its wholly-owned product candidate, tildacerfont, as the potential first non-steroidal therapy for patients suffering from classic congenital adrenal hyperplasia (CAH). Classic CAH is a serious and life-threatening disease with no known novel therapies approved in approximately 50 years. Spruce is also developing tildacerfont for women suffering from a rare form of polycystic ovary syndrome (PCOS) with primary adrenal androgen excess, representing 3-5% of females with PCOS (estimated to be 150,000 to 200,000 patients in the United States). To learn more, visit www.sprucebiosciences.com and follow us on Twitter @Spruce_Bio, LinkedIn and Facebook.

Forward-Looking Statements

Statements contained in this press release regarding matters that are not historical facts are “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. Such forward-looking statements include statements regarding, among other things, the results, conduct, progress and timing of Spruce’s clinical trials, the regulatory approval path for tildacerfont, the strength of Spruce’s balance sheet and the adequacy of Spruce’s cash position. Because such statements are subject to risks and uncertainties, actual results may differ materially from those expressed or implied by such forward-looking statements. Words such as “plans”, “will”, “believe”, “potential” and similar expressions are intended to identify forward-looking statements. These forward-looking statements are based upon Spruce’s current expectations and involve assumptions that may never materialize or may prove to be incorrect. Actual results could differ materially from those anticipated in such forward-looking statements as a result of various risks and uncertainties, which include, without limitation, risks and uncertainties associated with Spruce’s business in general, the impact of the COVID-19 pandemic, and the other risks described in Spruce’s filings with the U.S. Securities and Exchange Commission. All forward-looking statements contained in this press release speak only as of the date on which they were made and are based on management’s assumptions and estimates as of such date. Spruce undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made, except as required by law.

 

SPRUCE BIOSCIENCES, INC.

BALANCE SHEETS

(in thousands, except share amounts)

 

 

 

December 31,

 

 

2020

 

 

2019

 

ASSETS

 

 

 

 

 

 

Current assets:

 

 

 

 

 

 

Cash and cash equivalents

 

$

157,150

 

 

$

3,924

 

Prepaid expenses

 

 

2,971

 

 

 

215

 

Other current assets

 

 

276

 

 

 

513

 

Total current assets

 

 

160,397

 

 

 

4,652

 

Restricted cash

 

 

216

 

 

 

 

Right-of-use assets

 

 

1,793

 

 

 

 

Other assets

 

 

477

 

 

 

40

 

Total assets

 

$

162,883

 

 

$

4,692

 

LIABILITIES, REDEEMABLE CONVERTIBLE PREFERRED STOCK AND STOCKHOLDERS’ EQUITY (DEFICIT)

 

 

 

 

 

 

Current liabilities:

 

 

 

 

 

 

Accounts payable

 

$

3,628

 

 

$

1,878

 

Term loan, current portion

 

 

2,554

 

 

 

1,252

 

Accrued expenses and other current liabilities

 

 

2,496

 

 

 

265

 

Accrued compensation and benefits

 

 

1,085

 

 

 

908

 

Total current liabilities

 

 

9,763

 

 

 

4,303

 

Term loan, net of current portion

 

 

1,922

 

 

 

3,193

 

Lease liability, net of current portion

 

 

1,653

 

 

 

 

Other liabilities

 

 

118

 

 

 

20

 

Total liabilities

 

 

13,456

 

 

 

7,516

 

Series A redeemable convertible preferred stock, $0.0001 par value; 0 shares and 28,000,000 shares authorized, issued and outstanding as of December 31, 2020 and 2019, respectively; liquidation preference of $0 and $28,000 as of December 31, 2020 and 2019, respectively

 

 

 

 

 

27,813

 

Stockholders’ equity (deficit):

 

 

 

 

 

 

Preferred stock, $0.0001 par value; 10,000,000 shares and 0 shares authorized as of December 31, 2020 and 2019, respectively; 0 shares issued and outstanding as of December 31, 2020 and 2019

 

 

 

 

 

 

Common stock, $0.0001 par value; 200,000,000 shares and 41,000,000 shares authorized as of December 31, 2020 and 2019, respectively; 23,260,399 shares and 764,408 shares issued and outstanding as of December 31, 2020 and 2019, respectively

 

 

2

 

 

 

1

 

Additional paid-in capital

 

 

210,266

 

 

 

664

 

Accumulated deficit

 

 

(60,841

)

 

 

(31,302

)

Total stockholders’ equity (deficit)

 

 

149,427

 

 

 

(30,637

)

Total liabilities, redeemable convertible preferred stock and stockholders’ equity (deficit)

 

$

162,883

 

 

$

4,692

 

 

SPRUCE BIOSCIENCES, INC.

STATEMENTS OF OPERATIONS

(unaudited)

(in thousands, except share and per share amounts)

 

 

 

Three Months Ended

December 31,

 

Twelve Months Ended

December 31,

 

 

2020

 

 

2019

 

 

2020

 

 

2019

 

Operating expenses:

 

 

 

 

 

 

 

 

 

 

 

 

Research and development

 

$

5,813

 

 

$

2,847

 

 

$

23,854

 

 

$

10,817

 

General and administrative

 

 

2,521

 

 

 

286

 

 

 

5,562

 

 

 

2,290

 

Total operating expenses

 

 

8,334

 

 

 

3,133

 

 

 

29,416

 

 

 

13,107

 

Loss from operations

 

 

(8,334

)

 

 

(3,133

)

 

 

(29,416

)

 

 

(13,107

)

Interest expense

 

 

(79

)

 

 

(60

)

 

 

(323

)

 

 

(65

)

Other income, net

 

 

75

 

 

 

12

 

 

 

200

 

 

 

84

 

Net loss

 

$

(8,338

)

 

$

(3,181

)

 

$

(29,539

)

 

$

(13,088

)

Net loss per share, basic and diluted

 

$

(0.39

)

 

$

(4.16

)

 

$

(4.93

)

 

$

(17.12

)

Weighted-average shares of common stock outstanding, basic and diluted

 

 

21,542,045

 

 

 

764,408

 

 

 

5,991,213

 

 

 

764,408

 

 

FAQ

What were Spruce Biosciences' Q4 2020 financial results?

Spruce Biosciences reported a net loss of $8.3 million in Q4 2020.

What is the significance of the CAHmelia program for SPRB?

The CAHmelia program aims to change treatment for classic congenital adrenal hyperplasia, crucial for patient management.

What are the upcoming milestones for Spruce Biosciences?

Anticipated milestones include filing an IND application for PCOS and initiating Phase 2 trials in pediatric classic CAH.

How much cash did Spruce Biosciences have at the end of 2020?

The company reported cash and cash equivalents of $157.2 million as of December 31, 2020.

What were the R&D expenses reported by SPRB for 2020?

R&D expenses for 2020 were $23.9 million, significantly up from $10.8 million in 2019.

Spruce Biosciences, Inc.

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