Narazaciclib progressing towards registrational studies; target engagement and acceptable safety profile support further dose escalation, affirming differentiated profile
Update on the registrational preparations for the narazaciclib program and the rigosertib trial plan expected in the first half of 2024
Company to host conference call and webcast at
“Onconova has made excellent progress in the third quarter of 2023. Starting with our lead program, narazaciclib, a differentiated inhibitor of multiple kinases including CDK4/6, we advanced the registrational trial preparations in the first indication, for patients with low grade endometrioid endometrial cancer (LGEEC). CDK4/6 inhibitors have substantially changed the face of cancer care for the better and become a multibillion-dollar drug class. We believe narazaciclib has the potential to be differentiated by potently targeting proteins putatively involved in the resistance pathways of cancer cells that the approved agents fail to significantly inhibit,” said
“From a corporate perspective, in the third quarter, we named Dr.
Near Term Narazaciclib Milestones: Onconova intends to:
- present preclinical data at two December medical meetings: the San Antonio Breast Cancer Symposium (SABCS) and the annual meeting of the
American Society of Hematology (ASH); - continue the dose escalation segment of the Phase 1/2 program which may bring us into the first quarter of 2024;
- provide a read-out on narazaciclib’s safety and pharmacology in the first half of 2024;
- provide an update on our registrational trial-readiness over the next few quarters, including the definition of our recommended Phase 2 dose, engagement with the FDA on the pivotal trial design, and continuing to work with external clinical experts including the
Gynecologic Oncology Group (GOG), and theEuropean Network for Gynecologic Oncology Trials (ENGOT).
Achievement of these milestones will also enable us to establish a solid foundation to expand the program to include other indications such as breast cancer, ovarian cancer, and mantle cell lymphoma.
Rigosertib milestones: Onconova confirms plans to provide an update on the next steps to obtain orphan designation for rigosertib in RDEB-associated SCC and for the registrational program in the first half of 2024.
Second Quarter Financial Results
Cash and cash equivalents as of
Research and development expenses were
General and administrative expenses were
Net loss for the third quarter of 2023 was
Conference Call and Webcast Information
Interested parties who wish to participate in the conference call may do so by dialing:
- (800) 715-9871 for domestic and
- (646) 307-1963 for international callers and
- Using conference ID 3238751
Those interested in listening to the conference call via the internet may do so by visiting the investors and media page on the Company's website at www.onconova.com and clicking on the webcast link. In addition to the live webcast, a replay will be available on the Onconova website for 90 days following the call.
About
Narazaciclib, Onconova’s novel, multi-kinase inhibitor (formerly ON 123300), is being evaluated in a Phase 1/2 combination trial with the estrogen blocker letrozole, in advanced endometrial cancer (NCT05705505). Based on preclinical and clinical studies of CDK 4/6 inhibitors, Onconova believes narazaciclib has broad potential and is also evaluating opportunities for combination studies with narazaciclib and letrozole in additional indications, including breast cancer, ovarian cancer and mantle cell lymphoma.
Rigosertib is being studied in an investigator-sponsored trial strategy to evaluate the product candidate in multiple indications, including a dose-escalation and expansion Phase 1/2a study of oral rigosertib in combination with nivolumab in patients with KRAS+ non-small cell lung cancer (NCT04263090), a Phase 2 program evaluating oral or IV rigosertib monotherapy in advanced squamous cell carcinoma complicating recessive dystrophic epidermolysis bullosa (RDEB-associated SCC) (NCT03786237, NCT04177498), and a Phase 2 trial evaluating rigosertib in combination with pembrolizumab in patients with metastatic melanoma (NCT05764395).
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 its clinical development and trials, its product candidates, its business and financial position. Onconova has attempted to identify forward-looking statements by terminology including "believes," "estimates," "anticipates," "expects," "plans," "intends," "may," "could," "might," "will," "should," “preliminary,” “encouraging,” "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, investigator-initiated trials and regulatory agency and institutional review board approvals of protocols, 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:
267-759-3680
ir@onconova.us
https://www.onconova.com/contact/
Investor Contact:
646-889-1200
bmackle@lifesciadvisors.com
Condensed Consolidated Balance Sheets | |||||||
(in thousands) | |||||||
2023 | 2022 | ||||||
Assets | (unaudited) | ||||||
Current assets: | |||||||
Cash and cash equivalents | $ | 25,244 | $ | 38,757 | |||
Receivables | 18 | 29 | |||||
Prepaid expenses and other current assets | 1,749 | 561 | |||||
Total current assets | 27,011 | 39,347 | |||||
Property and equipment, net | 26 | 24 | |||||
Other non-current assets | 1 | 1 | |||||
Total assets | $ | 27,038 | $ | 39,372 | |||
Liabilities and stockholders' equity | |||||||
Current liabilities: | |||||||
Accounts payable | $ | 6,148 | $ | 3,860 | |||
Accrued expenses and other current liabilities | 3,300 | 3,960 | |||||
Deferred revenue | 226 | 226 | |||||
Total current liabilities | 9,674 | 8,046 | |||||
Deferred revenue, non-current | 2,847 | 3,017 | |||||
Total liabilities | 12,521 | 11,063 | |||||
Stockholders' equity: | |||||||
Preferred stock | - | - | |||||
Common stock | 210 | 209 | |||||
Additional paid in capital | 492,784 | 491,816 | |||||
Accumulated other comprehensive loss | (30 | ) | (33 | ) | |||
Accumulated deficit | (478,447 | ) | (463,683 | ) | |||
Total stockholders' equity | 14,517 | 28,309 | |||||
Total liabilities and stockholders' equity | $ | 27,038 | $ | 39,372 | |||
Condensed Consolidated Statements of Operations (unaudited) | |||||||||||||||
(in thousands, except share and per share amounts) | |||||||||||||||
Three Months Ended | Nine Months Ended | ||||||||||||||
2023 | 2022 | 2023 | 2022 | ||||||||||||
Revenue | $ | 57 | $ | 57 | $ | 170 | $ | 170 | |||||||
Operating expenses: | |||||||||||||||
General and administrative | 2,686 | 2,105 | 7,010 | 6,430 | |||||||||||
Research and development | 2,460 | 3,593 | 8,996 | 7,633 | |||||||||||
Total operating expenses | 5,146 | 5,698 | 16,006 | 14,063 | |||||||||||
Loss from operations | (5,089 | ) | (5,641 | ) | (15,836 | ) | (13,893 | ) | |||||||
Other income, net | 350 | 243 | 1,072 | 349 | |||||||||||
Net loss | (4,739 | ) | (5,398 | ) | (14,764 | ) | (13,544 | ) | |||||||
Net loss per share of common stock, basic and diluted | $ | (0.23 | ) | $ | (0.26 | ) | $ | (0.70 | ) | $ | (0.65 | ) | |||
Basic and diluted weighted average shares outstanding | 21,002,937 | 20,915,408 | 20,981,097 | 20,920,251 | |||||||||||
Source:
2023 GlobeNewswire, Inc., source