IDORSIA LTD Allschwil, Switzerland – October 22, 2019
Idorsia Ltd (SIX: IDIA) today announced its financial results for the first nine months of 2019.
Key figures
- US GAAP operating expenses 9M 2019 at CHF 375 million
- Non-GAAP operating expenses 9M 2019 at CHF 347 million
- Updated financial guidance for 2019: US GAAP operating expenses not to exceed CHF 540 million and non-GAAP operating expenses not to exceed CHF 500 million (both measures exclude any potential milestone payments)
Jean-Paul Clozel, MD and Chief Executive Officer, commented:
“Our clinical portfolio is making great progress. For our dual orexin receptor antagonist, daridorexant, we chose to run a broad and detailed registration program and we are very close to seeing the results of those activities. The first study is finishing recruitment, so we are confident that the results will be available in the first half of next year and the second study will follow shortly thereafter. This is a very exciting time at Idorsia as we prepare to deliver our scientific innovations to patients.”
Financial results
| US GAAP results | Nine Months | Third Quarter | ||
| in CHF millions, except EPS (CHF) and number of shares (millions) | 2019 | 2018 | 2019 | 2018 |
| Revenues | 20 | 20 | 7 | 7 |
| Operating expenses | (375) | (290) | (123) | (122) |
| Operating income (loss) | (355) | (271) | (116) | (115) |
| Net income (loss) | (352) | (278) | (120) | (119) |
| Basic EPS | (2.68) | (2.27) | (0.91) | (0.92) |
| Basic weighted average number of shares | 131.2 | 122.7 | 131.2 | 129.6 |
| Diluted EPS | (2.68) | (2.27) | (0.91) | (0.92) |
| Diluted weighted average number of shares | 131.2 | 122.7 | 131.2 | 129.6 |
US GAAP revenue of CHF 20 million in the first nine months of 2019 as well as 2018 related to deferred contract revenue recognized in connection to the collaboration agreements with Janssen (CHF 15.9 million) and Roche (CHF 3.8 million).
US GAAP operating expenses in the first nine months of 2019 amounted to CHF 375 million (of which CHF 327 million R&D and CHF 48 million SG&A expenses), whilst operating expenses in the first nine months of 2018 amounted to CHF 290 million (of which CHF 245 million R&D and CHF 45 million SG&A expenses).
US GAAP net loss in the first nine months of 2019 amounted to CHF 352 million compared to CHF 278 million for the first nine months of 2018. The increase of the net loss was mainly driven by higher operating costs.
The US GAAP net loss resulted in a net loss per share of CHF 2.68 (basic and diluted) for the first nine months of 2019 compared to a net loss per share of CHF 2.27 (basic and diluted) for the first nine months of 2018.
| Non-GAAP* measures | Nine Months | Third Quarter | ||
| in CHF millions, except EPS (CHF) and number of shares (millions) | 2019 | 2018 | 2019 | 2018 |
| Revenues | 20 | 20 | 7 | 7 |
| Operating expenses | (347) | (266) | (113) | (114) |
| Operating income (loss) | (328) | (247) | (107) | (107) |
| Net income (loss) | (326) | (249) | (104) | (109) |
| Basic EPS | (2.49) | (2.03) | (0.79) | (0.84) |
| Basic weighted average number of shares | 131.2 | 122.7 | 131.2 | 129.6 |
| Diluted EPS | (2.49) | (2.03) | (0.79) | (0.84) |
| Diluted weighted average number of shares | 131.2 | 122.7 | 131.2 | 129.6 |
* Idorsia measures, reports and issues guidance on non-GAAP operating performance. Idorsia believes that these non-GAAP financial measurements more accurately reflect the underlying business performance and therefore provide useful supplementary information to investors. These non-GAAP measures are reported in addition to, not as a substitute for, US GAAP financial performance.
Non-GAAP net loss in the first nine months of 2019 amounted to CHF 326 million: the difference versus US GAAP net loss was mainly due to depreciation and amortization (CHF 15 million), share-based compensation (CHF 13 million), and positive non-cash financial result (CHF 3 million).
The non-GAAP net loss resulted in a net loss per share of CHF 2.49 (basic and diluted) for the first nine months of 2019 compared to a net loss per share of CHF 2.03 (basic and diluted) for the first nine months of 2018.
André C. Muller, Chief Financial Officer, commented:
“In the first nine months of 2019 expenses were below our initial expectations, the result of lower clinical spend reflecting a slightly lower recruitment into some programs, but also a cost-conscious attitude from all our team. As a result, we are updating our financial guidance for 2019, now unforeseen events and potential milestone payments excluded, we expect non-GAAP operating expenses for 2019 not to exceed CHF 500 million.”
Liquidity and indebtedness
At the end of the first nine months of 2019, Idorsia’s liquidity (including cash, cash equivalents, short- and long-term deposits) amounted to CHF 875 million.
| (in CHF millions) | Sep 30, 2019 | Jun 30, 2019 | Mar 31, 2019 | Dec 31, 2018 |
| Liquidity | ||||
| Cash and cash equivalents | 385 | 467 | 718 | 799 |
| Short-term deposits | 210 | 219 | 94 | 123 |
| Long-term deposits | 280 | 318 | 300 | 298 |
| Total liquidity* | 875 | 1,004 | 1,111 | 1,220 |
| Indebtedness | ||||
| Convertible loan | 378 | 376 | 374 | 372 |
| Convertible bond | 199 | 199 | 199 | 198 |
| Other financial debt | - | - | - | - |
| Total indebtedness | 577 | 575 | 573 | 571 |
*rounding differences may occur
Clinical Development Pipeline
Idorsia has a diversified and balanced clinical development pipeline covering multiple therapeutic areas, including CNS, cardiovascular and immunological disorders, as well as orphan diseases.
The first Phase 3 registration study investigating daridorexant (25 and 50mg) for the treatment of adult and elderly patients with insomnia, ID-078A301, closed screening in October 2019. The study has a 3-month treatment period with a 1-month safety follow-up so, based on this progress, initial results are expected towards mid-2020.
Recruitment into the Phase 3 registration study with lucerastat for the treatment of patients with Fabry disease has passed the halfway mark but is slower than initially anticipated and the study is now expected to last into 2021.
Idorsia is making progress with its early development pipeline and is initiating a Phase 1 program with a new compound, ACT-1014-6470, intended to be developed in immunological disorders, towards the end of 2019.
Details of the pipeline can be found in our clinical development fact sheet.
Compound | Mechanism of Action | Target Indication | Status |
| Aprocitentan* | Dual endothelin receptor antagonist | Resistant hypertension management | Phase 3 |
| Clazosentan | Endothelin receptor antagonist | Vasospasm associated with aneurysmal subarachnoid hemorrhage | Phase 3 |
| Daridorexant | Dual orexin receptor antagonist | Insomnia | Phase 3 |
| Lucerastat | Glucosylceramide synthase inhibitor | Fabry disease | Phase 3 |
| Cenerimod | S1P1 receptor modulator | Systemic lupus erythematosus | Phase 2 |
| Selatogrel | P2Y12 receptor antagonist | Suspected acute myocardial infarction | Phase 2 |
| ACT-774312 | CRTH2 receptor antagonist | Nasal polyposis | Phase 2 |
| ACT-519276 | GBA2/GCS inhibitor | Rare CNS diseases | Phase 1 |
| ACT-539313 | Selective orexin 1 receptor antagonist | Psychiatric disorders | Phase 1 |
| ACT-709478** | T-type calcium channel blocker | Epilepsy | Phase 1 |
| ACT-1004-1239 | - | Immunology / Cancer Immunotherapy | Phase 1 |
| ACT-1014-6470 | - | Immunology | Initiating Phase 1 |
* In collaboration with Janssen Biotech Inc. to jointly develop and solely commercialize aprocitentan worldwide
** Idorsia has granted to a third party an option to license ACT-709478 and/or enter in a research collaboration for back-up or follow-on calcium channel blocker compounds; this option will expire 60 days after the IND submission to the FDA, which is planned for late 2019
Idorsia has the option to license vamorolone from ReveraGen Inc. and has granted to Santhera Holding Ltd. the option to sub-license vamorolone worldwide (except Japan and South-Korea) for all indications.
Results Day Center
Investor community: To make your job easier, we provide all relevant documentation via the Results Day Center on our corporate website: www.idorsia.com/results-day-center.
Upcoming Financial Updates
- Full-Year 2019 Financial Results reporting on February 6, 2020
- First Quarter 2020 Financial Results reporting on April 23, 2020
- Annual General Meeting of Shareholders on May 13, 2020
- Half-Year 2020 Financial Results reporting on July 23, 2020
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Notes to the editor
About Idorsia
Idorsia Ltd is reaching out for more - We have more ideas, we see more opportunities and we want to help more patients. In order to achieve this, we will develop Idorsia into one of Europe’s leading biopharmaceutical companies, with a strong scientific core.
Headquartered in Switzerland - a biotech-hub of Europe - Idorsia is specialized in the discovery and development of small molecules, to transform the horizon of therapeutic options. Idorsia has a broad portfolio of innovative drugs in the pipeline, an experienced team, a fully-functional research center, and a strong balance sheet – the ideal constellation to bringing R&D efforts to business success.
Idorsia was listed on the SIX Swiss Exchange (ticker symbol: IDIA) in June 2017 and has over 750 highly qualified specialists dedicated to realizing our ambitious targets.
For further information, please contact
Andrew C. Weiss
Senior Vice President, Head of Investor Relations & Corporate Communications
Idorsia Pharmaceuticals Ltd, Hegenheimermattweg 91, CH-4123 Allschwil
+41 58 844 10 10
www.idorsia.com
The above information contains certain "forward-looking statements", relating to the company's business, which can be identified by the use of forward-looking terminology such as "estimates", "believes", "expects", "may", "are expected to", "will", "will continue", "should", "would be", "seeks", "pending" or "anticipates" or similar expressions, or by discussions of strategy, plans or intentions. Such statements include descriptions of the company's investment and research and development programs and anticipated expenditures in connection therewith, descriptions of new products expected to be introduced by the company and anticipated customer demand for such products and products in the company's existing portfolio. Such statements reflect the current views of the company with respect to future events and are subject to certain risks, uncertainties and assumptions. Many factors could cause the actual results, performance or achievements of the company to be materially different from any future results, performances or achievements that may be expressed or implied by such forward-looking statements. Should one or more of these risks or uncertainties materialize, or should underlying assumptions prove incorrect, actual results may vary materially from those described herein as anticipated, believed, estimated or expected.
Attachment
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