ImmunoPrecise Reports Financial Results and Recent Business Highlights for Third Quarter Fiscal Year 2022
ImmunoPrecise Antibodies Ltd. (IPA) reported its Q3 fiscal 2022 results, achieving project revenue of $4.1 million, a rise of 22.6% year-over-year. Total revenue increased to $4.8 million, up 6.6%. The company invested $1.8 million in R&D, significantly higher than last year. However, it recorded a net loss of $3.8 million, worsening from a $1.3 million loss a year ago. As of January 31, 2022, cash reserves stood at $33.0 million.
- Project revenue grew by $0.7 million or 22.6% year-over-year.
- Total revenue increased by $0.3 million or 6.6% compared to last year.
- Investments in R&D rose to $1.8 million from nil, reflecting strategic growth.
- Polytope® TATX-03 is progressing well with no significant regulatory hurdles reported.
- Net loss increased to $3.8 million from $1.3 million year-over-year, indicating rising expenses.
- Product sales fell by 60.9% to $0.5 million, primarily due to the absence of previously sold therapeutic assets.
Third Quarter Fiscal Year 2022 Financial Summary*
(All comparisons are to the period ended
-
The Company achieved Project revenue of
, an increase of$4.1 million or$0.7 million 22.6% as compared to Project revenue of from the same year ago period.$3.3 million -
The Company’s total revenue of
was an increase of$4.8 million or$0.3 million 6.6% as compared to total revenue of from the same year ago period.$4.5 million -
The Company, primarily through its subsidiary
Talem Therapeutics LLC , invested in strategic research and development costs as compared to an investment of nil in the same year ago-period.$1.8 million -
The Company recorded a net loss of
, as compared to net loss of$3.8 million as compared to the same year-ago period.$1.3 million -
As of
January 31, 2022 , the Company held cash of .$33.0 million
*Expressed in Canadian dollars, unless otherwise indicated.
Dr.
“TATX-03, currently in pre-IND phase — is tracking well against development timelines. As such, we expect to submit an investigational new drug application (IND) with the FDA by the third quarter of the calendar year. A highlight of this development program has been the absence of any significant regulatory hurdles to date, as we believe IPA’s conservative development and working in lockstep with the FDA inquiry process has paid off. This is against the backdrop of a rapidly evolving regulatory framework required to address the shifting future landscape around the fight against COVID-19. In tandem to the Company’s independent development efforts, we have also recently announced a partnering agreement with Elektrofi, to participate in a
Recent Third Quarter Fiscal 2022 Operational Highlights
-
IPA was selected to work with Elektrofi on COVID-19 therapeutic delivery and future pandemic preparation under SBIR contract from
Defense Health Agency (DHA) within theUS Department of Defense -
Polytope® TATX-03 aggregate program update:
- No pharmacokinetic aberrations in in vivo animal model study.
- Injection with TATX-03 is well tolerated - with a significant safety margin and no clinical signs of toxicity.
- Maximum tolerated dose study evaluating up to a 12.5-fold higher amount than the highest dose anticipated for use in humans did not uncover any observable clinical signs of toxicity.
- SARS-CoV-2 PolyTope® antibody cocktail retains in vitro binding efficacy against viral variants-of-concern tested to date.
- Initiated assessment of retention of binding to cell-associated Omicron spike protein variant (B.1.1.529).
- Improved protein homogeneity in PolyTope® antibody cocktail for production purposes.
- Demonstrated in vitro pseudovirus assays, PolyTope® advanced immunotherapeutic TATX-03 prevents infection of cells by SARS-CoV-2 variant-of-concern, Omicron, and all variants of concern tested to date.
- Established manufacturing collaboration with ChemPartner Biologics for PolyTope® TATX-03 Antibody Cocktail.
-
Talem Therapeutic filed a non-provisional
U.S. patent application and concurrent international PCT (Patent Cooperation Treaty) and other national patent applications relating to the discovery of PolyTope® TATX-03, its in vitro and in vivo effects, and therapeutic use. -
Leased future new space for laboratory expansion at IPA Europe in a new multi-tenant biotech Center of Excellence at the Pivot Park Campus in Oss,
Netherlands .
Financial Results
Revenue
Project revenue of
The Company achieved revenue of
Product sales during the three months ended
Research & Development
Research and development increased to
Net Loss
The Company recorded a net loss of
Financing Activities / Liquidity and Capital Resources
As of
On
Webcast Details
Date:
Time:
Toll-free dial-in number: 1-877-407-3982
International dial-in number: 1-201-493-6780
Conference ID: 13727621
Webcast: https://viavid.webcasts.com/starthere.jsp?ei=1534157&tp_key=1be5e34d32
The conference call will be webcast live and available for replay via a link provided in the Investors section of the company’s website at https://www.immunoprecise.com/investors/.
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ImmunoPrecise is a biotherapeutic, innovation-powered company that supports its business partners in their quest to discover and develop novel antibodies against a broad range of target classes of diseases. The Company offers a hybrid of services and programs with advanced platforms and technologies — dynamic scientists and business advisors — to optimize antibody discovery and development, against rare and/or challenging epitopes. For further information, visit www.immunoprecise.com.
Forward Looking Information
This news release contains forward-looking statements within the meaning of applicable
Forward-looking information involves known and unknown risks, uncertainties and other factors which may cause the actual results, performance or achievements stated herein to be materially different from any future results, performance or achievements expressed or implied by the forward-looking information. Actual results could differ materially from those currently anticipated due to a number of factors and risks, including, without limitation, the Company may not be successful in developing its products through the successful and timely completion of preclinical assays, studies and clinical trials, or may not receive all regulatory approvals to commence and then continue clinical trials of its products, and, be successful in partnering or commercializing its products, including those related to COVID-19, the coverage and applicability of the Company’s intellectual property rights to its products, as well as those risks discussed in the Company’s Annual Information Form dated
The forward-looking statements contained in this news release are made as of the date of this release and, accordingly, are subject to change after such date. The Company does not assume any obligation to update or revise any forward-looking statements, whether written or oral, that may be made from time to time by us or on our behalf, except as required by applicable law.
**Non-IFRS Financial Measure
Readers are cautioned that "Adjusted EBITDA" is a measure not recognized under IFRS. Adjusted EBITDA is defined as operating earnings before interest, accretion, taxes, depreciation, amortization, share-based compensation, foreign exchange gain/loss, and asset impairment charges. Management believes Adjusted EBITDA is a useful measure that facilitates period-to-period operating comparisons. Readers are cautioned that "Adjusted EBITDA" is not an alternative to measures determined in accordance with IFRS and should not, on its own, be construed as indicator of performance, cash flow or profitability.
Neither the
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