Navidea Biopharmaceuticals Reports Second Quarter 2022 Financial Results
Navidea Biopharmaceuticals (NAVB) reported Q2 2022 financial results with net revenues of $57,000, down from $261,000 in Q2 2021. The net loss attributable to common stockholders widened to $3.0 million, or $0.10 per share, compared to a loss of $2.7 million, or $0.09 per share, in the same quarter last year. Ongoing Phase 3 trial enrollment for rheumatoid arthritis continues, alongside positive preliminary results from the NAV3-32 Phase 2b trial. The company closed a $2.5 million bridge loan and received $800,000 from a strategic partner for R&D expenses.
- Enrollment continues in NAV3-33 Phase 3 trial for rheumatoid arthritis.
- Positive preliminary results from NAV3-32 Phase 2b trial.
- Secured $800,000 from a strategic partner for R&D.
- Closed $2.5 million bridge loan.
- Net revenues decreased to $57,000 from $261,000 in Q2 2021.
- Net loss increased to $3.0 million, or $0.10 per share, from $2.7 million, or $0.09 per share in Q2 2021.
Conference Call to be Scheduled at a Later Date
Second Quarter 2022 Highlights and Subsequent Events
- Continued enrollment into the Company’s NAV3-33 Phase 3 trial in rheumatoid arthritis (“RA”) titled “Evaluation of Tc 99m Tilmanocept Imaging for the Early Prediction of Anti-TNFα Therapy Response in Patients with Moderate to Severe Active Rheumatoid Arthritis.” Enrollment is ongoing across the three currently opened sites.
- Announced positive preliminary results from the Company’s ongoing NAV3-32 Phase 2b trial comparing Tc99m tilmanocept imaging to histopathology of joints of patients with active RA. Two non-overlapping classes that align with the fibroid and non-fibroid histological pathotypes were identified, supporting the hypothesis that these classes can be identified by Tc99m tilmanocept imaging.
-
Received
from a strategic partner as reimbursement for certain manufacturing and research and development expenses.$800,000 -
The Company’s abstract titled “TAM Targeted Imaging Agents Binding CD206 and Selective Blocking of Off Target Liver Localization” was presented at the
Society of Nuclear Medicine and Molecular Imaging Annual Meeting onJune 11, 2022 inVancouver, British Columbia . -
The Company’s abstract titled “CD206 Targeted Delivery of Bisphosphonate Payloads Alter Human Macrophage Phenotypes Towards M1-like” was presented at the Tumor Myeloid-Directed Therapies Summit on
June 14, 2022 inBoston, MA. -
Announced publication of a manuscript titled “Increased Macrophage Specific Arterial Inflammation Relates Uniquely to Non-calcified Plaque and Specific Immune Activation Pathways in People with HIV: A Targeted Molecular Imaging Approach,” based on work performed at the
Massachusetts General Hospital (“MGH”) andHarvard Medical School ,Boston MA , and sponsored by the Company. The research, appearing inThe Journal of Infectious Diseases (PMID: 35856671), was led by Principal InvestigatorSteven Grinspoon , MD, Chief of the Metabolism Unit at MGH and Professor of Medicine atHarvard Medical School . -
Announced publication of a manuscript titled “Tilmanocept as a novel tracer for lymphatic mapping and sentinel lymph node biopsy in melanoma and oral cancer,” based on work performed at the
Crown Princess Mary Cancer Centre (“CPMCC”) at theUniversity of Sydney , inSydney, Australia . The research, appearing in theANZ Journal of Surgery (PMID: 35848587), was led by Principal Investigator Dr. Muzib Abdul-Razak, MBBS, FRACS, FRCSE, MCh., of the Faculty of Medicine,Department of Surgical Oncology and Head and Neck Surgery in the CPMCC at theUniversity of Sydney . - Received notification of issuance of patent from the USPTO for the application titled, “Compounds And Compositions For Treating Leishmaniasis And Methods Of Diagnosis And Treating Using Same” (Patent No. US 11,369,680 B2).
- Filed a provisional patent application describing a new degradable linker for dexamethasone and paclitaxel containing Manocept therapeutic constructs. These constructs are being evaluated preclinically for effects on macrophages and in animal models of oncology and inflammatory indications.
-
Received a Decision of Grant for patent application in
Japan for claims related to targeted delivery of a wide range of therapeutic payloads attached to Manocept platform-based constructs using a degradable hydrazone linker. -
Closed on a
bridge loan from the Company’s Vice Chair of the Board of Directors,$2.5 million John K. Scott , Jr. - Adopted a plan designed to protect the Company’s net operating loss and tax credit carryforwards.
Financial Results
-
Total net revenues for the second quarter of 2022 were
, compared to$57,000 for the same period in 2021. Total net revenues for the first half of 2022 were$261,000 , compared to$57,000 for the same period in 2021. The decrease was primarily due to the 2021 partial recovery of debts previously written off in 2015, the 2021 receipt of reimbursement from$385,000 Cardinal Health 414, LLC of certain research and development (“R&D”) costs, decreased grant revenue related toSmall Business Innovation Research grants from theNational Institutes of Health supporting Manocept development, and decreased license revenue from transitional sales of Tc99m tilmanocept inEurope . -
Research and development expenses for the second quarter of 2022 were
, compared to$1.7 million for the same period in 2021. R&D expenses for the first half of 2022 were$1.5 million , compared to$2.9 million for the same period in 2021. The increase was primarily due to increased employee compensation including incentive-based awards and increased recruiting fees, offset by decreases in drug project expenses and regulatory consulting expenses.$2.7 million -
Selling, general and administrative (“SG&A”) expenses for the second quarter of 2022 were
, compared to$1.3 million for the same period in 2021. SG&A expenses for the first half of 2022 were$1.4 million , compared to$3.1 million for the same period in 2021. Decreases in employee compensation including fringe benefits and incentive-based awards, travel, investor relations, general office expenses, facilities costs and franchise taxes were offset by increases in insurance, director fees, losses on the abandonment of certain intellectual property and legal and professional services.$3.7 million -
Navidea’s net loss attributable to common stockholders for the second quarter of 2022 was
, or$3.0 million per share, compared to$0.10 , or$2.7 million per share, for the same period in 2021. Navidea’s net loss attributable to common stockholders for the first half of 2022 was$0.09 , or$6.0 million per share, compared to$0.20 , or$5.6 million per share, for the same period in 2021.$0.20 -
Navidea ended the second quarter of 2022 with
in cash and cash equivalents.$328,000 million
The Company’s registration statement on Form S-1 (Registration No. 333-262691) relative to the Company's current rights offering was declared effective by the
This press release does not constitute an offer to sell or the solicitation of an offer to buy these securities, nor will there be any sale of these securities in any state or other jurisdiction in which such offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of any such state or jurisdiction.
In light of the Company’s pending rights offering, the Company will host a second quarter earnings conference call and business update following the conclusion of the rights offering. The Company will issue a press release announcing the date and time of the earnings conference call.
About Navidea
Forward-Looking Statements
This press release contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. We have based these forward-looking statements largely on our current expectations and projections about future events and financial trends affecting the financial condition of our business. Forward-looking statements include our expectations regarding pending litigation and other matters. These forward-looking statements are subject to a number of risks, uncertainties and assumptions, including, among other things: our history of operating losses and uncertainty of future profitability; the final outcome of any pending litigation; our ability to successfully complete research and further development of our drug candidates; the timing, cost and uncertainty of obtaining regulatory approvals of our drug candidates; our ability to successfully commercialize our drug candidates; dependence on royalties and grant revenue; our ability to implement our growth strategy; anticipated trends in our business; our limited product line and distribution channels; advances in technologies and development of new competitive products; our ability to comply with the NYSE American continued listing standards; our ability to maintain effective internal control over financial reporting; the impact of the current coronavirus pandemic; and other risk factors detailed in our most recent Annual Report on Form 10-K and other
Investors are urged to consider statements that include the words “will,” “may,” “could,” “should,” “plan,” “continue,” “designed,” “goal,” “forecast,” “future,” “believe,” “intend,” “expect,” “anticipate,” “estimate,” “project,” and similar expressions, as well as the negatives of those words or other comparable words, to be uncertain forward-looking statements.
You are cautioned not to place undue reliance on any forward-looking statements, any of which could turn out to be incorrect. We undertake no obligation to update publicly or revise any forward-looking statements, whether as a result of new information, future events or otherwise after the date of this report. In light of these risks and uncertainties, the forward-looking events and circumstances discussed in this report may not occur and actual results could differ materially from those anticipated or implied in the forward-looking statements.
CONDENSED CONSOLIDATED BALANCE SHEETS | ||||||||||||||||
|
|
|
||||||||||||||
2022 |
|
2021 |
||||||||||||||
(unaudited) | ||||||||||||||||
Assets: | ||||||||||||||||
Cash and cash equivalents | $ |
328,012 |
|
$ |
4,230,865 |
|
||||||||||
Other current assets |
|
842,728 |
|
|
1,152,420 |
|
||||||||||
Non-current assets |
|
1,332,965 |
|
|
1,261,548 |
|
||||||||||
Total assets | $ |
2,503,705 |
|
$ |
6,644,833 |
|
||||||||||
Liabilities and stockholders' (deficit) equity: | ||||||||||||||||
Current liabilities | $ |
5,321,985 |
|
$ |
5,299,802 |
|
||||||||||
Deferred revenue, non-current |
|
700,000 |
|
|
700,000 |
|
||||||||||
Note payable to related party, net of discount |
|
720,305 |
|
|
- |
|
||||||||||
Other liabilities |
|
2,062 |
|
|
20,288 |
|
||||||||||
Total liabilities |
|
6,744,352 |
|
|
6,020,090 |
|
||||||||||
Total stockholders' deficit |
|
(4,533,164 |
) |
|
(106,556 |
) |
||||||||||
Noncontrolling interest |
|
292,517 |
|
|
731,299 |
|
||||||||||
Total Navidea stockholders' (deficit) equity |
|
(4,240,647 |
) |
|
624,743 |
|
||||||||||
Total liabilities and stockholders' (deficit) equity | $ |
2,503,705 |
|
$ |
6,644,833 |
|
||||||||||
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS | ||||||||||||||||
Three Months Ended |
|
Six Months Ended |
||||||||||||||
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|
|
|
|
|
|
||||||||||
2022 |
|
2021 |
|
2022 |
|
2021 |
||||||||||
(unaudited) |
|
(unaudited) |
|
(unaudited) |
|
(unaudited) |
||||||||||
Revenue | $ |
57,526 |
|
$ |
261,046 |
|
$ |
57,526 |
|
$ |
384,783 |
|
||||
Cost of revenue |
|
473 |
|
|
- |
|
|
473 |
|
|
- |
|
||||
Gross profit |
|
57,053 |
|
|
261,046 |
|
|
57,053 |
|
|
384,783 |
|
||||
Operating expenses: | ||||||||||||||||
Research and development |
|
1,723,988 |
|
|
1,498,056 |
|
|
2,893,242 |
|
|
2,720,810 |
|
||||
Selling, general and administrative |
|
1,255,666 |
|
|
1,432,610 |
|
|
3,065,695 |
|
|
3,663,355 |
|
||||
Total operating expenses |
|
2,979,654 |
|
|
2,930,666 |
|
|
5,958,937 |
|
|
6,384,165 |
|
||||
Loss from operations |
|
(2,922,601 |
) |
|
(2,669,620 |
) |
|
(5,901,884 |
) |
|
(5,999,382 |
) |
||||
Other income (expense): | ||||||||||||||||
Interest (expense) income, net |
|
(83,584 |
) |
|
1,266 |
|
|
(87,246 |
) |
|
(1,609 |
) |
||||
Gain on extinguishment of debt |
|
- |
|
|
- |
|
|
- |
|
|
366,000 |
|
||||
Other, net |
|
6,726 |
|
|
(5,686 |
) |
|
2,427 |
|
|
(5,941 |
) |
||||
Net loss |
|
(2,999,459 |
) |
|
(2,674,040 |
) |
|
(5,986,703 |
) |
|
(5,640,932 |
) |
||||
Loss attributable to noncontrolling interest |
|
1 |
|
|
1 |
|
|
3 |
|
|
3 |
|
||||
Net loss attributable to common stockholders | $ |
(2,999,458 |
) |
$ |
(2,674,039 |
) |
$ |
(5,986,700 |
) |
$ |
(5,640,929 |
) |
||||
Loss attributable to common stockholders | ||||||||||||||||
per common share (basic and diluted) | $ |
(0.10 |
) |
$ |
(0.09 |
) |
$ |
(0.20 |
) |
$ |
(0.20 |
) |
||||
Weighted average shares outstanding (basic and diluted) |
|
30,268,858 |
|
|
29,117,832 |
|
|
30,238,471 |
|
|
28,531,660 |
|
View source version on businesswire.com: https://www.businesswire.com/news/home/20220814005023/en/
Investor Relations Contact
Vice President of Operations
614-822-2365
jsmith@navidea.com
Source:
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