Onconova Therapeutics Reports Full Year 2020 Financial Results, Provides Business Update

Rhea-AI Summary

Onconova Therapeutics, Inc. (NASDAQ: ONTX) announced its financial results for the year ended December 31, 2020, highlighting significant developments in its clinical pipeline. Key milestones include FDA clearance for Phase 1 studies of ON 123300, a multi-kinase inhibitor targeting advanced cancers. The company raised $35.2 million from equity offerings, bringing cash and equivalents to approximately $49.5 million. In 2020, Onconova reported a net loss of $25.2 million, equating to $0.14 per share. The company expects this funding will sustain operations and trials for over 18 months.

Positive

• FDA clearance received for Phase 1 studies of ON 123300.
• Raised $35.2 million from equity offerings.
• Cash and cash equivalents projected to last over 18 months.

Negative

• Net loss for 2020 increased to $25.2 million from $21.5 million in 2019.
• Higher research and development expenses at $16.9 million, up from $15.5 million in 2019.

Conference call begins at 4:30 p.m. Eastern time today

NEWTOWN, Pa., March 11, 2021 (GLOBE NEWSWIRE) -- Onconova Therapeutics, Inc. (NASDAQ: ONTX) (“Onconova”), a clinical-stage biopharmaceutical company focused on discovering and developing novel therapies for patients with cancer, announces financial results for the twelve months ended December 31, 2020 and provides a business update.

Highlights of the fourth quarter of 2020 and recent weeks include:

• ON 123300, Onconova’s proprietary multi-kinase inhibitor, received clearance from the U.S. Food and Drug Administration (FDA) to begin Phase 1 studies
• ON 123300 also received Institutional Review Board (IRB) approval at one U.S. clinical trial site
• The Phase 1 solid tumor study with ON 123300 in China is ongoing and continues to enroll patients
• Raised net proceeds of $35.2 million from two equity offerings; cash and cash equivalents as of February 28, 2021 were approximately $49.5 million
• An independent investigator-initiated study with oral rigosertib in combination with a PD-1 inhibitor in advanced KRAS mutated non-small cell lung cancer is ongoing
• A Special Meeting of Stockholders to consider changes to the capital structure of the Company will reconvene on April 1, 2021

Management Commentary
“The fourth quarter and recent weeks have been active and productive at Onconova as we continue to advance our lead product ON 123300 into the clinic,” said Steven M. Fruchtman, M.D., President and Chief Executive Officer of Onconova. “We submitted an Investigational New Drug application to the FDA for a Phase 1 study in advanced cancers including HR+/HER 2- metastatic breast cancer patients resistant to approved second-generation CDK 4/6 inhibitors. In December 2020, we received clearance from the FDA to begin the study, and have since received IRB approval at our first site. We expect the first patient to be enrolled in the second quarter of this year. Two further sites are in the study set-up process.

“This Phase 1 study will assess the safety, tolerability and pharmacokinetics of ON 123300 administered orally at increasing doses starting at 40 mg daily continuously.

“Our partner in China, HanX Pharmaceuticals, continues enrolling a similar patient population in a Phase 1 dose-escalation study with ON 123300 at two sites. The initial dose cohort has been completed and the second dose cohort is enrolling. We are pleased that ON 123300 appears to be well tolerated so far as no dose-limiting toxicities have been seen to date. The HanX study is dosing patients on a 21-day cycle. Collectively, the U.S. and China Phase 1 studies are expected to provide data regarding the safety profile of ON 123300 and potentially provide preliminary efficacy signals in patients with advanced cancer.”

Commenting on ongoing investigator-sponsored studies with oral rigosertib, the company’s RAS pathway inhibitor, Dr. Fruchtman added, “We are currently supporting investigator-initiated studies that are exploring the use of oral rigosertib for cancers driven by mutation of the RAS gene including a Phase 1 study in combination with a PD-1 inhibitor for patients with progressive K-RAS mutated non-small cell lung cancer.  This study is open and continues to enroll patients, with the objectives to identify the recommended Phase 2 dose and to characterize the safety profile of the combination treatment. Results are expected in 2021.

“In addition, an investigator-initiated Phase 1b/2 study with oral rigosertib monotherapy in advanced squamous cell carcinoma associated with recessive dystrophic epidermolysis bullosa is open.  A preclinical study is also evaluating oral rigosertib in clear cell renal carcinoma.  We anticipate additional investigator-initiated studies in RAS-driven cancers in combination with PD-1 inhibitors, including in metastatic melanoma. Other than the cost of supplying oral rigosertib to the investigators, Onconova does not expect to incur significant expense for these studies,” Dr. Fruchtman stated.

Full Year Financial Results
Cash and cash equivalents as of December 31, 2020 were $19.0 million, compared with $22.7 million as of December 31, 2019. Subsequent to the end of the quarter, the Company raised net proceeds of $35.2 million from two equity offerings with institutional investors.   The Company expects that its cash and cash equivalents as of February 28, 2021 will be sufficient to fund ongoing clinical trials and business operations for more than eighteen months.

Research and development expenses were $16.9 million for 2020, compared with $15.5 million for 2019. The increase was primarily related to higher regulatory consulting fees and manufacturing costs related to clinical supply for ON 123300, partially offset by lower expenses for the oral rigosertib combination program and the Phase 3 INSPIRE study in the 2020 period.

General and administrative expenses were $8.3 million for 2020, consistent with 2019. Lower personnel and stock compensation expenses in 2020 due to personnel reductions in the 2019 period were offset by higher pre-commercialization, insurance, and corporate legal and stockholder meeting expenses in the 2020 period.

Net loss for 2020 was $25.2 million, or $0.14 per share on 174.0 million weighted average shares outstanding, compared with a loss of $21.5 million, or $1.49 per share for 2019 on 14.4 million weighted average shares outstanding.

Conference Call and Webcast
Onconova will host an investment community conference call today beginning at 4:30 p.m. Eastern time, during which management will discuss financial results for 2020, provide a business update and answer questions. Interested parties can participate by dialing (855) 428-5741 (domestic callers) or (210) 229-8823 (international callers) and using conference ID 3863774.

A live webcast of the conference call will be available in the Investors & Media section of the Company's website at www.onconova.com. A replay of the webcast will be available on the Onconova website for 90 days following the call.

About Onconova Therapeutics, Inc.
Onconova Therapeutics is a clinical-stage biopharmaceutical company focused on discovering and developing novel therapies for patients with cancer. The Company has proprietary targeted anti-cancer agents designed to disrupt specific cellular pathways that are important for cancer cell proliferation.

Onconova’s novel, proprietary multi-kinase inhibitor ON 123300 is planned to begin a dose-escalation and expansion Phase 1 trial in the U.S. in 2Q21, and a dose-escalation and expansion Phase 1 trial is currently underway in China. Onconova’s product candidate oral rigosertib is currently in a dose-escalation and expansion Phase 1 investigator-initiated study targeting patients with KRAS+ lung adenocarcinoma in combination with nivolumab. In addition, Onconova continues to conduct preclinical work investigating rigosertib in COVID-19. For more information, please visit www.onconova.com.

Forward-Looking Statements
Some of the statements in this release are forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, Section 21E of the Securities Exchange Act of 1934, as amended, and the Private Securities Litigation Reform Act of 1995, and involve risks and uncertainties. These statements relate to Onconova’s expectations regarding the registered direct offering, its patents and clinical development plans including patient enrollment timelines and indications for its product candidates. Onconova has attempted to identify forward-looking statements by terminology including "believes," "estimates," "anticipates," "expects," "plans," "intends," "may," "could," "might," "will," "should," "approximately" or other words that convey uncertainty of future events or outcomes. Although Onconova believes that the expectations reflected in such forward-looking statements are reasonable as of the date made, expectations may prove to have been materially different from the results expressed or implied by such forward-looking statements. These statements are only predictions and involve known and unknown risks, uncertainties, and other factors, including the success and timing of Onconova's clinical trials and regulatory agency and institutional review board approvals of protocols, Onconova’s ability to continue as a going concern, the need for additional financing, Onconova’s collaborations, market conditions and those discussed under the heading "Risk Factors" in Onconova's most recent Annual Report on Form 10-K and quarterly reports on Form 10-Q. Any forward-looking statements contained in this release speak only as of its date. Onconova undertakes no obligation to update any forward-looking statements contained in this release to reflect events or circumstances occurring after its date or to reflect the occurrence of unanticipated events.

Company Contact:
Avi Oler
Onconova Therapeutics, Inc.
267-759-3680
ir@onconova.us
https://www.onconova.com/contact/

Investor Contact:
LHA Investor Relations
Kim Sutton Golodetz
212-838-3777
kgolodetz@lhai.com

(Tables to follow)

ONCONOVA THERAPEUTICS, INC.
Condensed Consolidated Balance Sheets
(in thousands)
	December 31,				December 31,
	2020				2019
Assets	(unaudited)
Current assets:
Cash and cash equivalents	$	19,025			$	22,726
Receivables	37				98
Prepaid expenses and other current assets	722				650
Total current assets	19,784				23,474
Property and equipment, net	52				50
Other non-current assets	150				150
Total assets	$	19,986			$	23,674
Liabilities and stockholders' equity
Current liabilities:
Accounts payable	$	4,833			$	4,271
Accrued expenses and other current liabilities	4,962				3,795
Deferred revenue	226				226
Total current liabilities	10,021				8,292
Warrant liability	321				113
Deferred revenue, non-current	3,469				3,695
Total liabilities	13,811				12,100
Stockholders' equity:
Preferred stock	-				-
Common stock	1,859				1,112
Additional paid in capital	432,858				413,879
Accumulated other comprehensive income (loss)	14				(18		)
Accumulated deficit	(428,556		)		(403,399		)
Total stockholders' equity	6,175				11,574
Total liabilities and stockholders' equity	$	19,986			$	23,674

ONCONOVA THERAPEUTICS, INC.
Condensed Consolidated Statements of Operations (unaudited)
(in thousands, except share and per share amounts)
	Year Ended December 31,
	2020				2019
	(unaudited)
Revenue	$	231			$	2,183
Operating expenses:
General and administrative	8,326				8,345
Research and development	16,898				15,537
Total operating expenses	25,224				23,882
Loss from operations	(24,993		)		(21,699		)
Change in fair value of warrant liability	(208		)		63
Other income, net	48				143
Net loss before income taxes	(25,153		)		(21,493		)
Income tax expense	4				10
Net loss	(25,157		)		(21,503		)
Net loss per share of common stock, basic and diluted	$	(0.14	)		$	(1.49	)
Basic and diluted weighted average shares outstanding	174,035,872				14,384,476

FAQ

What were Onconova's financial results for 2020?

Onconova reported a net loss of $25.2 million for 2020, or $0.14 per share.

What is the status of ON 123300 clinical trials?

ON 123300 received FDA clearance for Phase 1 studies and is currently enrolling patients in both the U.S. and China.

How much funding did Onconova raise recently?

Onconova raised $35.2 million from two equity offerings.

What is Onconova's cash position as of February 2021?

As of February 28, 2021, Onconova has approximately $49.5 million in cash and cash equivalents.

When will Onconova's Special Meeting of Stockholders occur?

The Special Meeting of Stockholders will reconvene on April 1, 2021.