Reviva Pharmaceuticals Holdings, Inc. Reports First Quarter 2022 Financial Results and Recent Business Highlights
Reviva Pharmaceuticals (RVPH) reported a net loss of approximately $7.4 million or $0.40 per share for Q1 2022, an increase from $0.9 million or $0.10 per share in Q1 2021. As of March 31, 2022, cash reserves totaled $23.4 million, down from $29.7 million at year-end 2021, but projected to fund operations until at least March 2023. The company has initiated a pivotal Phase 3 trial for its lead asset, brilaroxazine, targeting schizophrenia. Topline data is expected in mid-2023.
- Initiated pivotal Phase 3 RECOVER study for brilaroxazine in February 2022.
- Cash reserves of $23.4 million projected to fund operations through at least March 2023.
- Successfully launched over a dozen clinical trial sites in the U.S., with plans for international sites.
- Net loss increased to $7.4 million in Q1 2022 compared to $0.9 million in Q1 2021.
- Cash decreased from $29.7 million at the end of 2021 to $23.4 million in Q1 2022.
- Hosted key opinion leader (KOL) webinar on brilaroxazine for schizophrenia and other neuropsychiatric disorders led by industry thought leaders Leslie Citrome, MD & Larry Ereshefsky, PharmD
- Topline data for pivotal Phase 3 trial evaluating brilaroxazine for the treatment
of schizophrenia anticipated in mid-2023 -
-
CUPERTINO, Calif., May 16, 2022 (GLOBE NEWSWIRE) -- Reviva Pharmaceuticals Holdings, Inc. (NASDAQ: RVPH) (“Reviva” or the “Company”), a clinical-stage pharmaceutical company developing therapies that seek to address unmet medical needs in the areas of central nervous system (CNS), cardiovascular, metabolic, and inflammatory diseases, today reported financial results for the first quarter ended March 31, 2022 and summarized recent business highlights.
“In the first quarter, we continued to advance clinical development of Reviva’s lead asset, brilaroxazine with dosing of the first patient in the pivotal Phase 3 RECOVER study in February to assess the safety and efficacy in patients with schizophrenia,” said Laxminarayan Bhat, Ph.D., Founder, President, and CEO of Reviva. “Since that time, the team has successfully initiated more than a dozen sites across the US, with additional international sites on schedule to launch later this summer in both India and Europe. In early May, we hosted an informative KOL event where experts Leslie Citrome and Larry Ereshefsky provided an overview of unmet medical needs and therapeutic opportunities in schizophrenia and other neuropsychiatric disorders, followed by a Company overview of data supporting the clinical development strategy for brilaroxazine in schizophrenia.”
“While we plan to prioritize our efforts on schizophrenia in the near-term, Reviva is evaluating opportunities in additional chronic neuropsychiatric and pulmonary indications that arise from an underlying dysfunction in serotonin and dopamine signaling,” Dr. Bhat added. “Brilaroxazine has therapeutic potential in indications related to bipolar disorder, major depressive disorder (MDD), attention deficit hyperactive disorder (ADHD), pulmonary arterial hypertension (PAH) and idiopathic pulmonary fibrosis (IPF) and we remain active in seeking various non-dilutive financing opportunities, including partnerships, to explore these indications.”
First Quarter 2022 and Recent Business Highlights
- Hosted key opinion leader webinar on brilaroxazine for schizophrenia and other neuropsychiatric disorders, featuring presentations by Leslie Citrome, MD (New York Medical College) & Larry Ereshefsky, PharmD (Apex Innovative Sciences) (May 2022)
- Announced first patient dosed in pivotal Phase 3 study and long-term safety trial evaluating brilaroxazine for the treatment of schizophrenia (Feb 2022)
- Received FDA May Proceed Letter for pivotal Phase 3 clinical trial and long-term safety trial evaluating brilaroxazine for the treatment of schizophrenia (Jan 2022)
Anticipated Milestones and Events
- Topline data for pivotal Phase 3 trial evaluating brilaroxazine for the treatment of schizophrenia anticipated in mid-2023
- May initiate Phase 2a studies in bipolar disorder, major depressive disorder (MDD), attention deficit hyperactive disorder (ADHD), pulmonary arterial hypertension (PAH) and idiopathic pulmonary fibrosis (IPF) subject to the receipt of additional financing
- Pursue strategic partnership opportunities for the development of our pipeline
- Evaluate grant and other non-dilutive financing opportunities for product candidates from Federal and State Healthcare Agencies and Foundations
First Quarter 2022 Financial Results
The Company reported a net loss of approximately
As of March 31, 2022, the Company’s cash totaled approximately
Reviva believes that based on the current operating plan and financial resources, the Company’s cash as of March 31, 2022 will be sufficient to fund its current operating plans through at least March 2023.
About Reviva
Reviva is a clinical-stage biopharmaceutical company that discovers, develops and seeks to commercialize next-generation therapeutics for diseases representing unmet medical needs and burdens to society, patients, and their families. Reviva’s current pipeline focuses on the central nervous system, respiratory and metabolic diseases. Reviva’s pipeline currently includes two drug candidates, RP5063 (brilaroxazine) and RP1208. Both are new chemical entities discovered in-house. Reviva has been granted composition of matter patents for both RP5063 and RP1208 in the United States (U.S.), Europe, and several other countries.
Forward-Looking Statements
This press release contains certain 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 and the Private Securities Litigation Reform Act, as amended, including those relating to the Company’s RECOVER trial, product development, clinical and regulatory timelines and expenses, market opportunity, ability to raise sufficient funding, competitive position, possible or assumed future results of operations, business strategies, potential growth opportunities and other statements that are predictive in nature. These forward-looking statements are based on current expectations, estimates, forecasts and projections about the industry and markets in which we operate and management’s current beliefs and assumptions. These statements may be identified by the use of forward-looking expressions, including, but not limited to, “expect,” “anticipate,” “intend,” “plan,” “believe,” “estimate,” “potential,” “predict,” “project,” “should,” “would” and similar expressions and the negatives of those terms. These statements relate to future events or our financial performance and involve known and unknown risks, uncertainties, and other factors which may cause actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. Such factors include those set forth in the Company’s filings with the Securities and Exchange Commission. Prospective investors are cautioned not to place undue reliance on such forward-looking statements, which speak only as of the date of this press release. The Company undertakes no obligation to publicly update any forward-looking statement, whether as a result of new information, future events or otherwise.
Corporate Contact:
Reviva Pharmaceuticals Holdings, Inc.
Laxminarayan Bhat, PhD
www.revivapharma.com
Investor Relations Contact:
LifeSci Advisors, LLC
Bruce Mackle
bmackle@lifesciadvisors.com
REVIVA PHARMACEUTICALS HOLDINGS, INC.
CONDENSED CONSOLIDATED BALANCE SHEETS (UNAUDITED)
March 31, | December 31, | ||||||
2022 | 2021 | ||||||
Assets | |||||||
Cash | $ | 23,421,237 | $ | 29,687,944 | |||
Prepaid expenses and other current assets | 1,847,165 | 1,716,057 | |||||
Total Assets | $ | 25,268,402 | $ | 31,404,001 | |||
Liabilities and Stockholders' Equity | |||||||
Liabilities | |||||||
Accounts payable | $ | 1,425,834 | $ | 509,583 | |||
Accrued expenses and other current liabilities | 2,197,640 | 1,835,228 | |||||
Total current liabilities | 3,623,474 | 2,344,811 | |||||
Warrant liabilities | 283,720 | 372,730 | |||||
Total Liabilities | 3,907,194 | 2,717,541 | |||||
Stockholders' equity | |||||||
Common stock | 1,513 | 1,443 | |||||
Additional paid-in capital | 95,556,672 | 95,516,986 | |||||
Accumulated deficit | (74,196,977 | ) | (66,831,969 | ) | |||
Total stockholders' equity | 21,361,208 | 28,686,460 | |||||
Total Liabilities and Stockholders' Equity | $ | 25,268,402 | $ | 31,404,001 |
REVIVA PHARMACEUTICALS HOLDINGS, INC.
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS (UNAUDITED)
For the Three Months Ended March 31, 2022 and 2021
Three Months Ended March 31, | |||||||
2022 | 2021 | ||||||
Operating expenses | |||||||
Research and development | $ | 5,830,018 | $ | 391,161 | |||
General and administrative | 1,620,139 | 1,480,967 | |||||
Total operating expenses | 7,450,157 | 1,872,128 | |||||
Loss from operations | (7,450,157 | ) | (1,872,128 | ) | |||
Other income (expense) | |||||||
Gain on remeasurement of warrant liabilities | 89,010 | 923,480 | |||||
Interest and other income (expense), net | (232 | ) | 148 | ||||
Total other income (expense), net | 88,778 | 923,628 | |||||
Loss before provision for income taxes | (7,361,379 | ) | (948,500 | ) | |||
Provision for income taxes | 3,629 | 800 | |||||
Net loss | $ | (7,365,008 | ) | $ | (949,300 | ) | |
Net loss per share: | |||||||
Basic and diluted | $ | (0.40 | ) | $ | (0.10 | ) | |
Weighted average shares outstanding | |||||||
Basic and diluted | 18,466,586 | 9,231,737 |
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