Qualigen Therapeutics, Inc. Provides Update on Product Development Priorities and Reports Second Quarter and Six Month 2021 Financial Results
Qualigen Therapeutics (Nasdaq: QLGN) shifts focus to its oncology pipeline, including QN-247 and RAS-F, after receiving FDA feedback on its COVID-19 candidate, QN-165. The FDA requested more preclinical studies, prompting the pivot due to the crowded market. Q2 revenue rose 24% to $1.1 million, while the first half saw a 28% increase to $3.0 million. Net loss for Q2 was $5.3 million, down from $18.6 million in 2020. Cash equivalents stood at $15.2 million as of June 30, 2021. Qualigen aims to secure Orphan Drug status for QN-247, enhancing its market position in oncology.
- Q2 revenues increased 24% YoY to $1.1 million.
- First-half revenues rose 28% YoY to $3.0 million.
- Reduction in net loss for Q2 to $5.3 million from $18.6 million in 2020.
- Cash equivalents of approximately $15.2 million at June 30, 2021.
- Plans to seek Orphan Drug status for QN-247, which would provide market advantages.
- FDA requests additional preclinical studies for QN-165 delay clinical trials for COVID-19.
- Research and development expenses increased to $4.5 million for Q2 from $0.6 million in 2020.
CARLSBAD, Calif.,, Aug. 17, 2021 (GLOBE NEWSWIRE) -- Qualigen Therapeutics, Inc. (Nasdaq: QLGN) today announces its intention to prioritize its focus to its oncology pipeline that includes QN-247 and RAS-F. These plans follow feedback the Company received from the United States Food and Drug Administration regarding Qualigen’s investigational new drug (IND) application for one of its other compounds, QN-165, for the treatment of COVID-19 in hospitalized patients.
“Although the FDA requested that we perform additional pre-clinical toxicity and safety pharmacology studies before proceeding with clinical trials in COVID-19 patients, we believe that, given the time horizon which these suggested studies would require, coupled with the already very crowded COVID-19 vaccine and therapeutic landscape, the best and most prudent strategy for us at this time is to pivot to focusing primarily on our oncology pipeline that includes QN-247 and RAS-F assets for which we have already seen encouraging preclinical data,” commented Michael Poirier, Qualigen’s Chairman and Chief Executive Officer. “We appreciate the FDA’s guidance regarding our approach to QN-165, which helps us to solidify our priority to address unmet medical needs in treating cancer patients. We look forward to sharing ongoing progress with our shareholders.”
Qualigen also today announces its second quarter and six-months 2021 financial results and provides a recap of the highlights of the 2021 second quarter.
Highlights from the Quarter Ended June 30, 2021:
- Q2 revenues increased 24 percent to
$1.1 million , compared to$0.9 million in the same quarter of the previous year - First-half revenues increased 28 percent to
$3.0 million , compared to$2.4 million in the same six month period of the previous year - Cash equivalents of approximately
$15.2 million at June 30, 2021 - Continued our license and sponsored research agreements with the University of Louisville to evaluate the use of QN-247 with G-quadruplex binders.
- Qualigen plans to seek to obtain Orphan Drug status for QN-247 (with or without such binders) for one or more indications, such as pancreatic cancer, acute myeloid leukemia and pediatric neuroblastoma. Orphan Drug status, if obtained, would be expected to confer several advantages including faster review and increased market protection.
- Qualigen plans to seek to obtain Orphan Drug status for QN-247 (with or without such binders) for one or more indications, such as pancreatic cancer, acute myeloid leukemia and pediatric neuroblastoma. Orphan Drug status, if obtained, would be expected to confer several advantages including faster review and increased market protection.
- In May 2021, Qualigen announced that it had named Tariq Arshad, MD, MBA, to the newly-created position of Senior Vice President, Chief Medical Officer. Dr. Arshad brings more than 20 years of biotech and pharmaceutical experience to Qualigen.
- In June 2021, Qualigen announced that it was added to the Russell Microcap® Index. Membership in the Russell Microcap Index means automatic inclusion in certain growth and value indexes. FTSE Russell determines membership for its indexes primarily by objective, market-capitalization rankings as well as style attributes.
Second Quarter and Six Month Financial Highlights and Analysis
Revenues for the three months ended June 30, 2021 were
Revenues for the six month period ended June 30, 2021 were
For the three months ended June 30, 2021, we reported a net loss of
For the six months ended June 30, 2021, the Company reported a net loss of
License revenue during the six months ended June 30, 2021 was approximately
Research and development expenses increased to
General and administrative expenses increased to
As of June 30, 2021, we had
About Qualigen Therapeutics, Inc.
Qualigen Therapeutics, Inc.’s cancer therapeutics pipeline includes QN-247, RAS-F, and STARS. QN-247 (formerly referred to as ALAN) is a DNA coated gold nanoparticle cancer drug candidate that has the potential to target various types of cancer with minimal side effects; the nanoparticle coating technology is similar to the core nanoparticle coating technology used in our blood-testing diagnostic products. The foundational aptamer of QN-247, QN-165, is also a drug candidate for viral-based infectious diseases. (QN-165 was formerly referred to as AS1411.) RAS-F is a family of RAS oncogene protein-protein interaction inhibitor small molecules for preventing mutated RAS genes' proteins from binding to their effector proteins; preventing this binding could stop tumor growth, especially in pancreatic, colorectal, and lung cancers. STARS is a DNA/RNA-based treatment device candidate for removal from circulating blood of precisely targeted tumor-produced and viral compounds.
Forward-Looking Statements
This news release contains forward-looking statements by the Company that involve risks and uncertainties and reflect the Company's judgment as of the date of this release. These statements include those related to the Company's prospects and strategy for the development of therapeutic drug candidates. Actual events or results may differ from the Company's expectations. For example, there can be no assurance that preclinical or clinical development of the Company's drugs (including QN-247 and RAS-F, and deprioritized infectious-disease programs such as QN-165) or therapeutic devices will be completed on any projected timeline or will be successful; that the FDA will approve any of the Company’s IND applications; that any clinical trials will be approved to begin by or will proceed as contemplated by any projected timeline; that the Company will successfully develop any drugs (including QN-247 and RAS-F) or therapeutic devices; that future clinical trial data will be favorable or that such trials will confirm any improvements over other products or lack negative impacts; that any drugs or therapeutic devices will receive required regulatory approvals (including Orphan Drug status) or that they will be commercially successful; that patents will issue on the Company's owned and in-licensed patent applications; that such patents, if any, and the Company's current owned and inlicensed patents would prevent competition; that the Company will be able to procure or earn sufficient working capital to complete the development, testing and launch of the Company's prospective therapeutic products (including QN-247 and RAS-F, and any repositioning of QN-165); or that the Company will be able to maintain or expand market demand and/or market share for the Company's diagnostic products. The Company's stock price could be harmed if any of the events or trends contemplated by the forward-looking statements fails to occur or is delayed or if any actual future event otherwise differs from expectations. Additional information concerning these and other risk factors affecting the Company's business can be found in the Company's prior filings with the Securities and Exchange Commission, including its most recent Form 10-K, all of which available at www.sec.gov. The Company disclaims any intent or obligation to update these forward-looking statements beyond the date of this news release, except as required by law. This caution is made under the safe harbor provisions of the Private Securities Litigation Reform Act of 1995.
Investor Relations:
For further information: David Kugelman
Atlanta Capital Partners, LLC
(404) 856-9157 or (866) 692-6847 Toll Free - U.S. & Canada
dk@atlcp.com
Tony Schor
Investor Awareness, Inc.
(847) 971-0922
tony@investorawareness.com
QUALIGEN THERAPEUTICS, INC.
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
(Unaudited)
| For the Three Months Ended June 30, | For the Six Months Ended June 30, | |||||||||||||||
| 2021 | 2020 | 2021 | 2020 | |||||||||||||
| REVENUES | ||||||||||||||||
| Net product sales | $ | 1,117,935 | $ | 904,067 | $ | 2,538,776 | $ | 2,315,823 | ||||||||
| License revenue | — | — | 478,654 | — | ||||||||||||
| Collaborative research revenue | — | — | — | 45,000 | ||||||||||||
| Total revenues | 1,117,935 | 904,067 | 3,017,430 | 2,360,823 | ||||||||||||
| EXPENSES | ||||||||||||||||
| Cost of product sales | 916,624 | 807,922 | 2,119,103 | 1,799,574 | ||||||||||||
| General and administrative | 2,952,100 | 1,979,614 | 5,826,038 | 2,897,993 | ||||||||||||
| Research and development | 4,508,466 | 597,345 | 8,007,840 | 835,403 | ||||||||||||
| Sales and marketing | 135,543 | 88,844 | 272,129 | 181,106 | ||||||||||||
| Total expenses | 8,512,733 | 3,473,725 | 16,225,110 | 5,714,076 | ||||||||||||
| LOSS FROM OPERATIONS | (7,394,798 | ) | (2,569,658 | ) | (13,207,680 | ) | (3,353,253 | ) | ||||||||
| OTHER (INCOME) EXPENSE, NET | ||||||||||||||||
| Loss (gain) on change in fair value of warrant liabilities | (2,075,100 | ) | 16,201,400 | (4,198,000 | ) | 16,201,400 | ||||||||||
| Interest (income) expense, net | (12,718 | ) | 57,364 | (30,061 | ) | 148,121 | ||||||||||
| Other (income), net | (2,352 | ) | (250,114 | ) | (2,894 | ) | (251,272 | ) | ||||||||
| Total other (income) expense, net | (2,090,170 | ) | 16,008,650 | (4,230,955 | ) | 16,098,249 | ||||||||||
| LOSS BEFORE PROVISION FOR INCOME TAXES | (5,304,628 | ) | (18,578,308 | ) | (8,976,725 | ) | (19,451,502 | ) | ||||||||
| PROVISION (BENEFIT) FOR INCOME TAXES | 605 | 597 | 1,135 | (22 | ) | |||||||||||
| NET LOSS | $ | (5,305,233 | ) | $ | (18,578,905 | ) | $ | (8,977,860 | ) | $ | (19,451,480 | ) | ||||
| Net loss per common share, basic and diluted | $ | (0.18 | ) | $ | (2.12 | ) | $ | (0.31 | ) | $ | (2.71 | ) | ||||
| Weighted—average number of shares outstanding, basic and diluted | 28,850,451 | 8,746,250 | 28,510,014 | 7,174,233 | ||||||||||||
QUALIGEN THERAPEUTICS, INC.
CONDENSED CONSOLIDATED BALANCE SHEETS
(Unaudited)
| June 30, 2021 | December 31, 2020 | |||||||
| ASSETS | ||||||||
| Current assets | ||||||||
| Cash and cash equivalents | $ | 15,232,402 | $ | 23,976,570 | ||||
| Accounts receivable, net | 766,911 | 615,757 | ||||||
| Inventory, net | 1,073,335 | 953,458 | ||||||
| Prepaid expenses and other current assets | 2,033,857 | 2,678,894 | ||||||
| Total current assets | 19,106,505 | 28,224,679 | ||||||
| Right-of-use assets | 321,076 | 430,795 | ||||||
| Property and equipment, net | 253,261 | 247,323 | ||||||
| Equipment held for lease, net | 5,821 | 17,947 | ||||||
| Intangible assets, net | 183,933 | 187,694 | ||||||
| Other assets | 18,334 | 18,334 | ||||||
| Total Assets | $ | 19,888,930 | $ | 29,126,772 | ||||
| LIABILITIES AND STOCKHOLDERS’ EQUITY | ||||||||
| Current liabilities | ||||||||
| Accounts payable | $ | 784,474 | $ | 500,768 | ||||
| Accrued expenses and other current liabilities | 1,923,708 | 746,738 | ||||||
| Notes payable, current portion | — | 131,766 | ||||||
| Deferred revenue, current portion | 325,988 | 486,031 | ||||||
| Operating lease liability, current portion | 270,640 | 254,739 | ||||||
| Warrant liabilities | 4,112,100 | 8,310,100 | ||||||
| Total current liabilities | 7,416,910 | 10,430,142 | ||||||
| Notes payable, net of current portion | — | 6,973 | ||||||
| Operating lease liability, net of current portion | 98,145 | 236,826 | ||||||
| Deferred revenue, net of current portion | 112,057 | 158,271 | ||||||
| Total liabilities | 7,627,112 | 10,832,212 | ||||||
| Stockholders’ equity | ||||||||
| Series Alpha convertible preferred stock, | 1 | 1 | ||||||
| Common stock, | 28,902 | 27,296 | ||||||
| Additional paid-in capital | 88,058,267 | 85,114,755 | ||||||
| Accumulated deficit | (75,825,352 | ) | (66,847,492 | ) | ||||
| Total stockholders’ equity | 12,261,818 | 18,294,560 | ||||||
| Total Liabilities and Stockholders’ Equity | $ | 19,888,930 | $ | 29,126,772 | ||||
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