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Kinarus Therapeutics Holding AG / Key word(s): Half Year Results
31-Aug-2022 / 07:00 CET/CEST
Release of an ad hoc announcement pursuant to Art. 53 LR
The issuer is solely responsible for the content of this announcement.
Ad hoc announcement pursuant to Art. 53 LR
- Interim data from Phase 2 KINETIC clinical trial of KIN001 to treat hospitalized COVID-19 patients expected in Q3 2022
- First patient dosed with in Phase 2 KINFAST clinical trial with ambulatory COVID-19 mild-patients
- Signed a CHF 20 million financing with Yorkville Advisors
- Fully financed until Q1 2023
Basel, Switzerland, August 31, 2022 – Kinarus Therapeutics Holding AG (SIX: KNRS), a clinical-stage biopharmaceutical company developing novel therapeutics to treat viral, respiratory and ophthalmic diseases, today reported results for the six months ended June 30, 2022, and provided a corporate update.
Dr. Alexander Bausch, CEO of Kinarus Therapeutics Holding AG, commented: “We believe we are well positioned to execute on multiple value-creating milestones. As a first of many, our experienced team is working to deliver in Q3 2022 interim results from our KINFAST Phase 2 clinical trial with hospitalized COVID-19 patients”.
“We continue to explore various financing options to support initiation of our Phase 2 clinical trials in wet AMD and IPF before the end of 2022,” Dr. Bausch continued, “We recently signed a financing deal with Yorkville Advisors, which would allow Kinarus to draw down funds opportunistically to finance our clinical development programs and further strengthen our balance sheet.”
Earlier this month Kinarus held and published on its website a webinar on KIN001’s potential to treat COVID-19 (https://ir.kinarus.com/reports-presentations/#presentations).
H1 2022 and Subsequent Highlights
- Completed a Reverse Takeover (“RTO”) transaction between Perfect Holding SA and Kinarus AG and the combined company, Kinarus Therapeutics’ shares resumed trading on SIX Swiss Exchange (“SIX”) from 3 June 2022. Through listing on SIX, Kinarus Therapeutics’ shareholders were able to find some liquidity and the Group would be able to access additional sources of funding to finance its clinical development programs.
- Received a recommendation from Data and Safety Monitoring Board (“DSMB”), following its interim safety review, to continue with the KINETIC Phase 2 clinical trial in hospitalized COVID-19 patients.
- Was issued US Patent No. 11285155 covering the pharmaceutical composition of KIN001 and its use in certain types of cancers, conferring protection until at least 2037.
- Signed a TCHF 20’000 financing agreement with Yorkville Advisors to draw down funds by issuing convertible notes over the next 36 months.
- Dosed the first patient in KINFAST Phase 2 clinical trial with ambulatory COVID-19 patients. An interim readout from the trial is expected in H1 2023.
Analysis of Financial Statements for the Six Months Ended June 30, 2022
- Cash Position: The Company had a cash balance of TCHF 4’583. This compares to a cash balance of TCHF 124 as of December 31, 2021. The Company’s cash balance provides enough capital resources to progress through Q1 2023 without consideration of any financing proceeds or grant payments.
- R&D Expenditures: Our research and development expenses totalled TCHF 236 for the six months ended June 30, 2022. The expenses were attributable to our ongoing KINETIC Phase 2 clinical trial in hospitalized COVID-19 patients, the preparation of KINFAST Phase 2 clinical trial with ambulatory COVID-19 patients, production of drug products for the clinical studies, engagement of a clinical research organization to conduct the clinical trials, pre-clinical studies for the follow-on indications in our pipeline as well as expenses related to new IP filing and maintenance of existing IP.
- G&A Expenditures: For the six months ended June 30, 2022, G&A increased by TCHF 173 to TCHF 416. This increase is mostly related to one-off costs of TCHF 295 associated with RTO transaction expenses, hiring of additional consultants, insurance costs related to D&O insurance coverage for members of board and management, payment of board fees and costs related to increased public and investor relations activities.
- Financial Income: The Company recognized TCHF 131 in financial income related to the partial waiver of a bridge loan facility by a related party linked to one of the Group’s shareholders, a decrease of TCHF 149 compared to the prior period.
- Loss for the Period: The Company reported a net loss after taxes of TCHF 822 for the six months ended June 30, 2022, compared with a net profit of TCHF 33 for the comparable period in 2021.
Interim consolidated income statement (in TCHF)
| TCHF |
Notes |
01.01.22 - 30.06.22 |
01.01.21 - 30.06.21 |
| |
|
|
|
| External research and development expenses |
|
(236) |
- |
| Payroll expenses |
6 |
(107) |
- |
| General and administrative expenses |
7 |
(416) |
(243) |
| Loss before financial result, taxes and depreciation and amortization |
|
(759) |
(243) |
| Amortization of intangible assets |
12 |
(217) |
- |
| Financial income |
8 |
131 |
280 |
| Financial expenses |
8 |
(6) |
(4) |
| Exchange differences |
8 |
1 |
- |
| (Loss)/profit before taxes |
|
(850) |
33 |
| Income tax income/(expenses) |
|
28 |
- |
| (Loss)/profit for the period |
|
(822) |
33 |
| |
|
|
|
| (Loss)/profit attributable to: |
|
|
|
| Owners of the parent company |
|
(795) |
33 |
| Minority interests |
|
(27) |
- |
| |
|
(822) |
33 |
| |
|
|
|
| |
|
|
|
| (Loss)/profit per share |
|
|
|
| Basic and diluted (loss)/profit per share (in CHF) |
9 |
(0.0026) |
0.0002 |
| |
|
|
|
Interim consolidated balance sheet (in TCHF)
| TCHF |
Notes |
30 June 2022 |
31 December 2021 |
| |
|
|
|
| ASSETS |
|
|
|
| |
|
|
|
| Cash and cash equivalents |
|
4’583 |
124 |
| Other current assets |
10 |
174 |
12 |
| Current assets |
|
4’757 |
136 |
| |
|
|
|
| Property, plant and equipment |
11 |
9 |
- |
| Intangible assets |
12 |
51’880 |
- |
| Non-current assets |
|
51’889 |
- |
| Total assets |
|
56’646 |
136 |
| |
|
|
|
| |
|
|
|
| LIABILITIES AND EQUITY |
|
|
|
| |
|
|
|
| Trade account payables |
13 |
342 |
86 |
| Current provisions |
17.5 |
1’140 |
- |
| Other current liabilities |
14 |
869 |
21 |
| Current liabilities |
|
2’351 |
107 |
| |
|
|
|
| Non-current borrowings |
15 |
3’478 |
429 |
| Non-current prepayments |
16 |
4’400 |
- |
| Deferred tax liabilities |
|
6’510 |
- |
| Non-current liabilities |
|
14’388 |
429 |
| Total liabilities |
|
16’739 |
536 |
| |
|
|
|
| Share capital |
17.1 |
10’695 |
1’810 |
| Share premium |
|
30’475 |
220 |
| Treasury shares |
17.2 |
(1) |
- |
| Accumulated losses |
|
(3’225) |
(2’430) |
| Total equity attributable to owners of the parent company |
|
37’944 |
(400) |
| Minority interests |
|
1’963 |
- |
| Total equity |
|
39’907 |
(400) |
| Total liabilities and equity |
|
56’646 |
136 |
Kinarus Therapeutics Holding AG (www.kinarus.com) was founded in 2017 by experienced pharmaceutical executives in Basel, Switzerland. The Kinarus team utilizes its knowledge and drug development competencies to in-license and develop mid-stage clinical assets in which they have identified an increased probability of clinical and regulatory success and a rapid path to market. Kinarus possesses the exclusive worldwide license to pamapimod, covering all indications, and has patented KIN001, its novel mechanism in combination with pioglitazone.
Contacts
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Kinarus Therapeutics Holding AG
Hochbergerstrasse 60C
4057 Basel, Switzerland
+41 61 633 29 71
info@kinarus.com
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Investors & Media
Chris Maggos
BioConfidant Sàrl
+41 79 367 6254
maggos@bioconfidant.ch
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Legal disclaimer
THIS PRESS RELEASE DOES NOT CONSTITUTE AN OFFER TO SELL NOR AN INTIMATION TO SUBMIT A PROPOSAL FOR THE ACQUISITION OF SECURITIES OF KINARUS THERAPEUTICS HOLDING AG. THIS PRESS RELEASE IS NOT FOR RELEASE, PUBLICATION OR DISTRIBUTION, DIRECTLY OR INDIRECTLY, IN WHOLE OR IN PART, INTO OR WITHIN ANY JURISDICTION WHERE IT IS UNLAWFUL TO BE DISTRIBUTED.
End of Inside Information
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