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bioAffinity Technologies Reports Fourth Quarter and Full Year 2022 Financial Results Conference Call Scheduled for

Key Takeaway: bioAffinity Technologies reported its financial results for Q4 and the full year 2022, highlighting significant capital raises totaling approximately $13.8 million. The company achieved promising results in its clinical validation trial for CyPath Lung, which generated $2,500 in revenue during Q4. Despite these positive developments, bioAffinity recorded a net loss of $8.2 million for the year. The company is managing a pivotal trial to seek FDA clearance and is expanding its diagnostic capabilities to include additional lung diseases.

Market Sentiment Analysis

POSITIVE FACTORS

  • bioAffinity Technologies raised approximately $6.0 million from an IPO, enhancing financial stability.
  • The clinical validation trial for CyPath Lung showed promising sensitivity and specificity results.
  • The company plans to expand its product pipeline to include other lung diseases.
  • New appointments to the Scientific and Medical Advisory Board enhance research capabilities.

CONCERNS & RISKS

  • The company reported a net loss of $8.2 million for 2022, indicating ongoing financial challenges.
  • The increase in administrative expenses reflects growing operational costs linked to IPO compliance.

Full Press Release Details

Technologies Reports Fourth Quarter and Full Year 2022 Financial Results
Call Scheduled for April 3, 2023, at 9:00 a.m. Eastern Time
ANTONIO, Texas (March 31, 2023) - bioAffinity Technologies, Inc. (Nasdaq: BIAF; BIAFW), a biotechnology company addressing
the need for noninvasive detection of early-stage lung cancer and other diseases of the lung, today reported financial results for the
three and 12 months ended December 31, 2022.
Raised net proceeds of approximately $6.0 million from an initial public offering (IPO) in September 2022
Converted nearly $16 million in debt, related accrued interest and fair value adjustments into shares of common stock in connection with the IPO
Raised an additional $7.8 million from the exercise of warrants and stock options
and Operational Highlights
Announced publication in Respiratory Research of an article titled "Detection of early-stage lung cancer in sputum using automated flow cytometry and machine learning" detailing results of bioAffinity Technologies' clinical validation trial, which showed CyPath Lung had 92% sensitivity and 87% specificity in high-risk patients with nodules smaller than 20 millimeters or no nodules in the lung, with an area under the ROC curve of 94%
Selected a contract research organization to manage the pivotal trial intending to seek U.S. Food and Drug Administration clearance of CyPath Lung as a Class II IVD medical device for the detection of lung cancer; the pivotal trial is expected to recruit 1,800 patients beginning in 2023, with participants followed for at least one year to determine the presence of lung cancer
Research continues aimed at the expansion of the Company's flow cytometric platform technology for use in detecting additional lung diseases, including Chronic Obstructive Pulmonary Disease (COPD)
Announced publication in the Journal of Visualized Experiments of an article titled "Porphyrin-Modified Beads for Use as Compensation Controls in Flow Cytometry" describing the beads engineered by the Company for use with its CyPath Lung test
Received Notice of Allowance for a U.S. patent protecting the targeted delivery of novel cancer treatments using porphyrin compounds for bioAffinity Technologies' wholly owned subsidiary, OncoSelect Therapeutics
Awarded therapeutic patents in China, Mexico and Australia for compounds comprised of porphyrins conjugated to chemotherapeutic agents that can provide selective treatment for cancer; the Company's global patent portfolio now includes the U.S., Australia, Canada, China, France, Germany, Hong Kong, Italy, Mexico, Spain, Sweden and the United Kingdom
Expanded the Company's Scientific and Medical Advisory Board with the appointments of Sheila Habib, M.D., Director of the Pulmonary Lung Nodule Clinic and the Lung Cancer Screening Program at South Texas Veterans Health Care, and David Hill, M.D., National Board Member of the American Lung Association and assistant clinical professor of medicine at Yale University School of Medicine
Strengthened the diagnostics division with the appointment of Rossella Titone, Ph.D., and Alvaro Souto Padron de Figueiredo, Ph.D., who bring significant technical expertise in flow cytometry and clinical research across various cancers
Appointed Julie Anne Overton, a veteran of print and broadcast journalism, corporate communications and federal public affairs, as Director of Communications
Scheduled to ring the Nasdaq closing bell on April 5 to commemorate the Company's 2022 IPO
the capital raised during and following our IPO, 2022 was a landmark year for bioAffinity Technologies as we executed on our goal to
become a leader in non-invasive early-stage cancer diagnosis by bringing our first flow cytometry-based diagnostic, CyPath
Lung, to market. With key research and leadership appointments, we are engaging clinicians and patients on the value of early lung
cancer screening, lowering healthcare costs and raising the survival rate for one of the deadliest cancers," said Maria Zannes,
President and Chief Executive Officer of bioAffinity Technologies.
computed tomography (LDCT) is the standard of care for screening patients at high risk for lung cancer and can significantly increase
survival by finding early-stage cancer. But screening's low positive predictive rate of 3.8% means that only four people out of
100 who get a positive screening result will actually have lung cancer. CyPath Lung assists clinical decision-making
for patients whose screening results are not clear. Physicians can order bioAffinity's patient-friendly CyPath
Lung test to confirm or rule out cancer, reducing the need for biopsy and other costly invasive procedures, and providing greater clarity
to determine next steps in patient care.
ongoing pilot launch of CyPath Lung in Texas continues to provide value by helping us to refine positioning, gather valuable
insights from labs and healthcare providers, and optimize logistics throughout the care pathway, from ordering the test to reporting
results. By building upon real-world feedback from this test market, we are enhancing the value proposition of CyPath
Lung and can achieve more impactful adoption as we prepare for commercial expansion," Ms. Zannes said.
Quarter Financial Results
for the fourth quarter of 2022 was approximately $2,500, compared with no revenue for the prior-year period. Revenue was derived from
the sale of CyPath Lung as a Laboratory Developed Test (LDT).
and development expenses were $429,000 for the fourth quarter of 2022, compared with $318,000 for the comparable period in 2021. General
and administrative expenses were $1.2 million for the fourth quarter of 2022, compared with $341,000 for the comparable period in 2021.
loss for the fourth quarter of 2022 was $1.7 million, compared with a net loss of $5.6 million for the comparable period in 2021.
Year Financial Results
for 2022 was approximately $5,000, compared with no revenue for 2021.
and development expenses were $1.1 million in 2022, compared with $1.0 million in 2021. The increase was primarily due to higher personnel,
legal and research costs, partially offset by lower stock-based compensation expense.
and administrative expenses were $2.7 million in 2022, compared with $1.1 million in 2021. The increase was primarily due to higher consulting,
legal and professional fees related to the Company's IPO and compliance with public company reporting requirements. The increase
was also attributed to higher stock-based compensation expense, as well as hiring-related expenses to support the commercial launch of
loss for 2022 was $8.2 million, or $1.81 per share, compared with a net loss for 2021 of $6.3 million, or $2.36 per share.
and cash equivalents as of December 31, 2022, were $11.4 million. On September 6, 2022, bioAffinity Technologies raised net proceeds
of $6.0 million from an IPO of 1,282,600 units, with each unit consisting of one share of common stock, one tradeable warrant to purchase
one share of common stock and one non-tradable warrant. An additional $7.8 million was raised from the exercise of warrants and options.
bioAffinity Technologies believes that its available cash will be sufficient to fund planned operations for at least the next 12 months.
will host a conference call on Monday, April 3, 2023, at 9:00 a.m. Eastern time to discuss those results and answer questions.
Date: Monday, April 3, 2023
Time: 9:00 a.m. Eastern time
Toll Free: 877-270-2148
International: 412-902-6510
Webcast: Webcast link
replay of the event will be available for 90 days at the webcast link above, which can also be found in the Investor Relations section
of bioAffinity Technologies' website at ir.bioaffinitytech.com.
bioAffinity Technologies, Inc.
Technologies, Inc. addresses the need for noninvasive diagnosis of early-stage cancer and diseases of the lung, and targeted cancer treatment.
The Company's first product, CyPath Lung, is a noninvasive test that has shown high sensitivity and specificity
for the detection of early-stage lung cancer. CyPath Lung is marketed as a Laboratory Developed Test (LDT) by Precision
Pathology Services. OncoSelect Therapeutics , LLC, a subsidiary of bioAffinity Technologies, is advancing its discoveries
shown in vitro to kill cancer cells without harm to normal cells. Research and optimization of the Company's platform technologies
are conducted in its laboratories at The University of Texas at San Antonio. For more information, visit www.bioaffinitytech.com.
press release contains forward-looking statements, including statements regarding the anticipated use of proceeds from the Company's
offering of common shares. Forward-looking statements can be identified by words such as "believes," "expects,"
"estimates," "intends," "may," "plans," "will" and similar expressions, or
the negative of these words. Such forward-looking statements are based on facts and conditions as they exist at the time such statements
are made and predictions as to future facts and conditions. Readers of this press release are cautioned not to place undue reliance on
any forward-looking statements. The Company does not undertake any obligation to update any forward-looking statement relating to matters
discussed in this press release, except as may be required by applicable securities laws.
December 31,
2022 2021
ASSETS
Current assets:
Cash and cash equivalents $ 11,413,759 $ 1,360,638
Accounts and other receivables, net 10,489 1,530
Inventory 5,540 -
Prepaid expenses and other current assets 531,899 76,065
Total current assets 11,961,687 1,438,233
Deferred offering costs - 7,942
Property and equipment, net 214,438 4,633
Other assets 6,000 2,500
Total assets $ 12,182,125 $ 1,453,308
LIABILITIES, CONVERTIBLE PREFERRED STOCK, AND STOCKHOLDERS' EQUITY (DEFICIT)
Current liabilities:
Accounts payable $ 345,042 $ 230,407
Accrued expenses 541,894 483,501
Accrued interest - 1,121,392
Current portion of Paycheck Protection Program loan - 52,074
Loan payable 251,746 -
Convertible notes payable at fair value - 11,152,151
Total current liabilities 1,138,682 13,039,525
Paycheck Protection Program loan, less current portion - 160,184
Total liabilities 1,138,682 13,199,709
Commitments and contingencies
Convertible preferred stock, par value $0.001 per share; 20,000,000 shares authorized; 0 and 756,558 shares issued and outstanding, aggregate liquidation preference of $0 and $5,825,648 at December 31, 2022 and 2021, respectively - 4,044,318
Stockholders' equity (deficit):
Preferred stock, no shares issued or outstanding at December 31, 2022 and 2021, respectively - -
Common Stock, par value $0.007 per share; 14,285,714 shares authorized; 8,381,324 and 2,677,140 shares issued and outstanding as of December 31, 2022 and 2021, respectively 58,669 18,740
Additional paid-in capital 47,652,242 12,703,896
Accumulated deficit (36,667,468 ) (28,513,355 )
Total stockholders' equity (deficit) 11,043,443 (15,790,719 )
Total liabilities, convertible preferred stock, and stockholders' equity (deficit) $ 12,182,125 $ 1,453,308
Statements of Operations
the Years Ended December 31, 2022 and 2021
2022 2021
Revenue $ 4,803 $ -
Cost of sales 467 -
Gross profit 4,336 -
Operating expenses:
Research and development 1,142,777 1,007,476
Clinical development 145,546 130,475
Selling, general and administrative 2,727,071 1,068,871
Total operating expenses 4,015,394 2,206,822
Loss from operations (4,011,058 ) (2,206,822 )
Other income (expense):
Interest income 46,708 424
Interest expense (2,532,640 ) (1,001,854 )
Gain on extinguishment of debt 212,258 239,200
Fair value of warrants issued - (4,080,339 )
Fair value adjustments on convertible notes payable (1,866,922 ) 724,928
Loss before income taxes (8,151,654 ) (6,324,463 )
Income tax expense (2,459 ) (1,950 )
Net loss $ (8,154,113 ) $ (6,326,413 )
Net loss per common share, basic and diluted $ (1.81 ) $ (2.36 )
Weighted average common shares outstanding 4,498,964 2,675,270

Frequently Asked Questions

What were bioAffinity Technologies' 2022 financial results?

The company reported $5,000 in revenue for 2022, a decrease from prior losses.

What is CyPath Lung?

CyPath Lung is a noninvasive test designed for early-stage lung cancer detection.

What is the sensitivity of CyPath Lung?

CyPath Lung demonstrated 92% sensitivity and 87% specificity in clinical trials.

How much did the IPO raise for bioAffinity?

The IPO raised approximately $6.0 million, along with additional funds from warrants.

When will the pivotal trial for CyPath Lung begin?

The pivotal trial is scheduled to start in 2023, recruiting 1,800 patients.

Last updated: Apr 3, 2023