Spruce Biosciences Reports First Quarter 2022 Financial Results and Provides Corporate Update
Spruce Biosciences (Nasdaq: SPRB) reported progress in its CAHmelia-203 study for adult classic congenital adrenal hyperplasia (CAH), achieving 25% enrollment and expects topline data by H2 2023. The company amended its debt facility with Silicon Valley Bank for a $10 million credit line, reducing interest rates. R&D expenses rose to $8.5 million, while total operating expenses increased to $11.7 million, resulting in a net loss of $11.8 million for Q1 2022. The patent portfolio for tildacerfont has also expanded, enhancing market exclusivity.
- Achieved 25% enrollment in CAHmelia-203 study, on track for H2 2023 topline data.
- Amended debt facility with Silicon Valley Bank to provide a $10 million credit line, reducing interest rates.
- Expanded patent portfolio for tildacerfont, extending market exclusivity through 2038.
- R&D expenses increased to $8.5 million, up from $6.7 million.
- Total operating expenses rose to $11.7 million, compared to $9.8 million, contributing to increased net loss.
- Net loss for Q1 2022 was $11.8 million, up from $9.9 million in Q1 2021.
Debt Facility with Silicon Valley Bank Amended to Provide Up to
Tildacerfont Patent Portfolio Estate Expanded with
“Throughout the first quarter of 2022, we continued to drive our clinical and business objectives forward, with key progress made in our lead program for adults with classic congenital adrenal hyperplasia (CAH), expansion of our executive leadership team, and through potential access to non-dilutive sources of capital. We were pleased to achieve the recent milestone of
Recent Corporate & Pipeline Updates
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25% Enrollment Achieved in CAHmelia-203 Study for Adult Classic CAH:Spruce Biosciences recently achieved25% enrollment in the company’s CAHmelia-203 clinical study and is on track to report topline data in the second half of 2023. CAHmelia-203 is a randomized, double-blind, placebo-controlled, dose-ranging study evaluating the safety and efficacy of tildacerfont in adult patients with classic CAH and is designed to enroll approximately 72 patients with high levels of androstenedione (A4) on their current glucocorticoid regimen. Study sites are now enrolling under the amended protocol, which is anticipated to accelerate patient enrollment.
- Enrollment in CAHmelia-204 Progressing Under Amended Protocol: CAHmelia-204 is a randomized, double-blind, placebo-controlled study evaluating the safety and efficacy of tildacerfont in adult patients with classic CAH. The study is designed to enroll approximately 90 patients on supraphysiologic doses of glucocorticoids at or above 30 mg/d hydrocortisone equivalent with normal or near normal levels of A4. Study sites are now enrolling under the amended protocol, which removed the glucocorticoid conversion requirement. Enrollment is progressing as planned and the company plans to share enrollment updates over the course of the year.
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Debt Facility with
Silicon Valley Bank (SVB) Amended to Provide$10 Million Credit Line in 2022:Spruce Biosciences has amended its debt facility with SVB to provide a credit line of up to (“Tranche 2”) in 2022, subject to the satisfaction of certain financial and operating conditions. The amendment also reduces the current variable interest rate on the outstanding debt of$10 million by 50 basis points and on Tranche 2 by 250 basis points. Additionally, subject to potential drawdowns under Tranche 2 occurring, the interest-only period for outstanding term debt will be extended from$5 million December 31, 2022 toJune 30, 2023 . No warrants were issued in connection with the amended debt facility.
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Tildacerfont Patent Portfolio Estate Expanded with
Key Method of Use Patents:Spruce Biosciences continues to expand its patent portfolio for its wholly-owned product candidate tildacerfont to supplement its issued composition of matter patent and market exclusivity afforded by orphan drug designation inthe United States andEurope for CAH, if approved. InApril 2022 , the United States Patent and Trademark Office issuedU.S. Patent Number 11,304,950 titled “Methods of treating testicular and ovarian adrenal rest tumors,” andU.S. Patent Number 11,311,549 titled “Corticotropin release factor receptor antagonists.” The newly issued patents cover broad claims regarding the use of a CRF-1 receptor antagonist for the treatment of adrenal rest tumors and use of tildacerfont to reduce androstenedione in patients with CAH. These patents expand existing patent exclusivity through 2038.
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Libbie Mansell , Ph.D., M.B.A., R.A.C., Appointed Chief Regulatory and Quality Officer: InApril 2022 ,Libbie Mansell , Ph.D., M.B.A., R.A.C. was appointed Chief Regulatory and Quality Officer ofSpruce Biosciences , and will lead the company’s global regulatory affairs and quality strategy.Dr. Mansell is a seasoned regulatory affairs professional, with over 30 years of industry experience in serious and rare diseases. She joins Spruce fromAsklepios BioPharmaceutical (AskBio), where she served as Senior Vice President of Regulatory Affairs. Dr. Mansell’s appointment follows theMarch 2022 appointment ofWill Charlton , M.D., M.A.S., as Chief Medical Officer.
Upcoming Corporate Access Events
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RBC Capital Markets Global Healthcare Conference
Date:May 17-18, 2022
Format: Fireside chat (May 17 at10:00 a.m. ET ) and 1x1 meetings
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H.C. Wainwright Global Investment Conference
Date:May 23-26, 2022
Format: Company presentation (May 25 at4:00 p.m. ET ) and 1x1 meetings
Upcoming Medical Conferences
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24th
European Congress of Endocrinology (ECE 2022)
Date:May 21-24, 2022
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104th Annual Meeting of the
Endocrine Society (ENDO 2022)
Date:June 11-14, 2022
Anticipated Upcoming Milestones
- Completion of enrollment from the Phase 2 proof of concept clinical trial in PCOS by the end of 2022 and topline results in the first half of 2023
- Topline safety results from cohort 1 of the Phase 2 pediatric classic CAH clinical trial in the first half of 2023
- Topline results from the CAHmelia-203 clinical trial in adult classic CAH patients with elevated levels of A4 (labeled as in poor disease control) in the second half of 2023
- Topline results from the CAHmelia-204 clinical trial in adult classic CAH patients on supraphysiologic doses of glucocorticoids with normal or near normal levels of A4 (labeled as in good disease control) in the second half of 2024
First Quarter 2022 Financial Results
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Cash, Cash Equivalents and Investments: Cash, cash equivalents and investments as of
March 31, 2022 , were .$108.9 million
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Research and Development (R&D) Expenses: R&D expenses for the quarter ended
March 31, 2022 were compared to$8.5 million for the same period in 2021. The overall increase in R&D expenses was primarily related progressing clinical development of tildacerfont in adult classic CAH and the initiation of clinical programs in pediatric classic CAH and polycystic ovary syndrome.$6.7 million
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General and Administrative (G&A) Expenses: G&A expenses for the quarter ended
March 31, 2022 were compared to$3.2 million for the same period in 2021.$3.1 million
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Total Operating Expenses: Total operating expenses for the quarter ended
March 31, 2022 were , compared to$11.7 million for the same period in 2021. Stock-based compensation expense for the quarters ended$9.8 million March 31, 2022 and 2021 was and$1.1 million , respectively. When excluding depreciation and stock-based compensation expenses, non-GAAP total operating expenses for the quarters ended$1.1 million March 31, 2022 and 2021 were and$10.6 million , respectively.$8.7 million
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Net Loss: Net loss for the quarter ended
March 31, 2022 was compared to$11.8 million for the same period in 2021.$9.9 million
About
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 enrollment, results, conduct, progress and timing of Spruce’s clinical trials and announcements regarding the same, and the funding of Spruce’s operations. 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 “expect,” “anticipate”, “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
Use of Non-GAAP Financial Measures
Spruce has presented certain non-GAAP financial measures in this release. This release and the reconciliation table included herein include non-GAAP total operating expenses, which excludes depreciation and stock-based compensation. Spruce excludes depreciation and stock-based compensation because management believes the exclusion of these items is helpful to investors to evaluate Spruce's recurring operational performance. Spruce management uses this non-GAAP financial measure to monitor and evaluate its operating results and trends on an on-going basis, and internally for operating, budgeting and financial planning purposes. This non-GAAP financial measure should be considered in addition to results prepared in accordance with GAAP but should not be considered a substitute for or superior to GAAP results.
CONDENSED BALANCE SHEETS (in thousands, except share amounts) |
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ASSETS |
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(unaudited) |
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Current assets: |
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Cash and cash equivalents |
|
$ |
23,343 |
|
|
$ |
42,748 |
|
Short-term investments |
|
|
68,005 |
|
|
|
46,221 |
|
Prepaid expenses |
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|
3,423 |
|
|
|
2,530 |
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Other current assets |
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|
325 |
|
|
|
396 |
|
Total current assets |
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95,096 |
|
|
|
91,895 |
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Restricted cash |
|
|
216 |
|
|
|
216 |
|
Right-of-use assets, net |
|
|
1,397 |
|
|
|
1,479 |
|
Long-term investments |
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|
17,601 |
|
|
|
32,459 |
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Other assets |
|
|
678 |
|
|
|
437 |
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Total assets |
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$ |
114,988 |
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$ |
126,486 |
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LIABILITIES AND STOCKHOLDERS’ EQUITY |
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Current liabilities: |
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Accounts payable |
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$ |
1,109 |
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$ |
2,823 |
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Term loan, current portion |
|
|
405 |
|
|
|
— |
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Accrued expenses and other current liabilities |
|
|
6,457 |
|
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4,613 |
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Accrued compensation and benefits |
|
|
998 |
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1,435 |
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Total current liabilities |
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8,969 |
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|
8,871 |
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Term loan, net of current portion |
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|
4,485 |
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|
|
4,878 |
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Lease liability, net of current portion |
|
|
1,196 |
|
|
|
1,293 |
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Other liabilities |
|
|
95 |
|
|
|
73 |
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Total liabilities |
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14,745 |
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|
|
15,115 |
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Stockholders’ equity: |
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Preferred stock, |
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— |
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— |
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Common stock, |
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3 |
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3 |
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Additional paid-in capital |
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215,828 |
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214,685 |
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Accumulated other comprehensive loss |
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(693 |
) |
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(184 |
) |
Accumulated deficit |
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(114,895 |
) |
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(103,133 |
) |
Total stockholders’ equity |
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100,243 |
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|
111,371 |
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Total liabilities and stockholders’ equity |
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$ |
114,988 |
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$ |
126,486 |
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CONDENSED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS (unaudited) (in thousands, except share and per share amounts) |
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Three Months Ended
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2022 |
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2021 |
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Operating expenses: |
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Research and development |
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$ |
8,508 |
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$ |
6,714 |
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General and administrative |
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3,225 |
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3,103 |
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Total operating expenses |
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11,733 |
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|
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9,817 |
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Loss from operations |
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(11,733 |
) |
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(9,817 |
) |
Interest expense |
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(87 |
) |
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(89 |
) |
Other income, net |
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58 |
|
|
|
19 |
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Net loss |
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$ |
(11,762 |
) |
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$ |
(9,887 |
) |
Unrealized loss on available for sale securities |
|
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(509 |
) |
|
|
— |
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Comprehensive loss |
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$ |
(12,271 |
) |
|
$ |
(9,887 |
) |
Net loss per share, basic and diluted |
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$ |
(0.50 |
) |
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$ |
(0.42 |
) |
Weighted-average shares of common stock outstanding, basic and diluted |
|
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23,492,295 |
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23,283,658 |
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Reconciliation of Total Operating Expenses to Non-GAAP Total Operating Expenses (unaudited) (in thousands) |
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Three Months Ended |
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2022 |
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2021 |
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Operating expenses: |
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Total operating expenses |
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$ |
11,733 |
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$ |
9,817 |
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Adjustments: |
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Depreciation |
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9 |
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4 |
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Stock-based compensation |
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1,141 |
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|
|
1,120 |
|
Non-GAAP total operating expenses |
|
$ |
10,583 |
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$ |
8,693 |
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View source version on businesswire.com: https://www.businesswire.com/news/home/20220511005912/en/
Media Contact:
(619) 961-8848
will@canalecomm.com
media@sprucebiosciences.com
Investors
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investors@sprucebiosciences.com
Source:
FAQ
What is the progress of the CAHmelia-203 study for SPRB?
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How much is the amended credit line from Silicon Valley Bank for SPRB?