Chordate Medical carries out a rights issue of units of approximately SEK 41.8 million

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The Board of Directors of Chordate Medical Holding AB (publ) (“Chordate Medical” or the “Company") has today, subject to subsequent approval by the extraordinary general meeting in the Company on 26 January 2024, resolved to carry out a rights issue of units, consisting of shares and warrants, with preferential rights for the Company’s existing shareholders (the "Rights Issue"). The Rights Issue is mainly intended to finance (i) market registration and product versions, (ii) supporting clinical studies, (iii) market strategy activities and (iv) other working capital. In connection with the Rights Issue, the Company has received subscription undertakings of approximately SEK 10.7 million, corresponding to approximately 25.7 per cent of the Rights Issue. Furthermore, the Company has received guarantee commitments of approximately SEK 12.3 million, corresponding to approximately 29.3 per cent of the Rights Issue, which, in aggregate, is covered by subscription undertakings and guarantee commitments of approximately SEK 23.0 million in total, corresponding to approximately 55.0 per cent of the Rights Issue. In the Rights Issue, one (1) existing share entitles to subscription of one (1) unit where each unit consists of two (2) shares and one (1) warrant series TO 8. The subscription price is SEK 0.18 per unit. Provided that the Rights Issue is fully subscribed, Chordate Medical will receive initial proceeds of approximately SEK 41.8 million before issue costs. The Rights Issue is subject to approval by the extraordinary general meeting on 26 January 2024. Notice to the extraordinary general meeting will be published through a separate press release. Due to the Rights Issue, the Board of Directors of Chordate Medical has resolved to postpone the publication of the year-end report for 2023, from 29 February 2024 to 22 March 2024.

"During the fall, Chordate has successfully taken steps forward in the Company's commercial progress, continued to present the Company's impressive study and its results. Chordate has also initiated the pilot study PM009 and the post market surveillance study PM010 with renowned specialist clinics. Our treatment for migraine, Ozilia, is attracting great interest where we are receiving clear signals of purchase interest from relevant customers. Awareness of the treatment is also beginning to establish itself at very satisfactory levels. The need for Ozilia as a drug-free treatment alternative for migraine is evident. Chordate has now entered the final phase of building value in the company for a potential exit. The Board of Directors, our employees and I truly appreciate the support of our investors and look forward to taking the next exciting step in the company's development.", says Anders Weilandt, CEO of Chordate Medical.

Background and reasons
Chordate Medical Holding AB (publ) is a Swedish company that, through its wholly owned subsidiary Chordate Medical AB, develops, sells and markets Ozilia® (formerly K.O.S, Kinetic Oscillation Stimulation), a patented and CE-marked nerve stimulation technology for the treatment of chronic migraine and chronic rhinitis.

Ozilia® is a preventive and drug-free treatment of chronic migraine and chronic rhinitis. Several clinical studies have together reported few unexpected side effects. The Company's study, PM007, evaluated the effect of treatment with Ozilia® compared with placebo as a monthly reduction in the number of headache days with moderate to severe intensity. 132 patients at nine clinics in Germany and Finland were included. The primary endpoint showed a significant difference in mean headache days of -2.23 days (p=0.013) among patients receiving active treatment compared to placebo treatment. The completed study results provide support for marketing activities, such as customer meetings and working with early reimbursement solutions from public payers or private health insurance, in the migraine markets where the Company has chosen to operate, and in the ongoing work with the Company's FDA application.

The market for treatments for migraine is larger than the market for treatments for rhinitis, which is why success in the migraine area is a significant step in Chordate Medical's exit strategy (sale of the Company), which consists of three parts:

  • Broad patent portfolio – Chordate Medical has 74 granted patents grouped into 9 patent families covering various inventions in 24 markets and 2 additional patent applications are filed.
  • Invest in scientific evidence – The second part of the strategy is to produce scientifically based evidence of the treatment's clinical efficacy for the two indications.
  • Proof of concept – The third part is to show early market penetration in selected markets to demonstrate the value of the technology.

The Board of Directors makes the assessment that the existing working capital is not sufficient to conduct operations in the coming twelve-month period. To finance the Company and accelerate the work towards an exit (sale of the Company), primarily through continued investments in the migraine market with the latest study results as a starting point, the Board of Directors has decided to carry out the Rights Issue.

Provided that the Rights Issue is fully subscribed, the Company will initially receive approximately SEK 41.8 million before issue costs, which are expected to amount to approximately SEK 5.7 million. The net proceeds from the Rights Issue thus amount to approximately SEK 36.2 million. The Rights Issue is mainly intended to finance (i) market registration and product versions, (ii) supporting clinical studies, (iii) market strategy activities and (iv) other working capital.

In November 2024, the Company may receive additional proceeds if the warrants of series TO 8 issued in the Rights Issue are exercised for subscription of shares. Upon full subscription and full exercise of all warrants of series TO 8 within the framework of the issued units, the Company may receive an additional capital contribution of approximately SEK 34.9 million, based on a maximum subscription price of SEK 0.15. The proceeds from the exercise of warrants of series TO 8 are primarily intended to finance (i) market registration and product versions, (ii) supporting clinical studies, (iii) market strategy activities and (iv) other working capital.

Terms and conditions of the Rights Issue
The Board of Directors has today, subject to approval by the extraordinary general meeting on 26 January 2024, resolved to carry out the Rights Issue by issuing a maximum of 232,416,507 units. The right to subscribe for units with preferential rights shall vest in those who are registered as shareholders in the Company on the record date, 31 January 2024, whereby one (1) existing share entitles to one (1) unit right and one (1) unit right entitle to subscription of one (1) unit consisting of two (2) shares and one (1) warrant of series TO 8. In total, the Rights Issue comprises a maximum of 464,833,014 shares and a maximum of 232,416,507 warrants of series TO 8. The subscription price is SEK 0.18 per unit corresponding to a subscription price of SEK 0.09 per share, which means that Chordate Medical, provided that the Rights Issue is fully subscribed, initially will receive approximately SEK 41.8 million before issue costs and excluding the additional proceeds that may be received upon exercise of the warrants that are issued in the Rights Issue. The warrants are issued free of charge. Subscription of units with or without preferential rights shall take place during the period 2 February 2024 – 16 February 2024. Unit rights that are not utilized during the subscription period will become invalid and lose their value. Trading in unit rights is expected to take place on Nasdaq First North Growth Market during the period 2 February 2024 – 13 February 2024.

One (1) warrant of series TO 8 entitles the rights to subscribe for one (1) new share in the Company to a subscription price corresponding to seventy (70) per cent of the volume weighted average price of the Company’s share during the period from and including 16 October 2024 up to and including 29 October 2024, however not lower than the shares’ quota value and not more than SEK 0.15. Subscription of shares by exercise of warrants will take place during the period from and including 4 November 2024 up to and including 18 November 2024.

If not all units are subscribed for by exercise of unit rights, allotment of the remaining units shall be made within the highest amount of the Rights Issue: firstly, to those who have subscribed for units by exercise of unit rights (regardless of whether they were shareholders on the record date or not) and who have applied for subscription of units without exercise of unit rights and if allotment to these cannot be made in full, allotment shall be made pro rata in relation to the number of unit rights that each and every one of those, who have applied for subscription of units without exercise of unit rights, have exercised for subscription of units; secondly, to those who have subscribed for units in the Rights Issue without exercise of unit rights and if allotment to these cannot be made in full, allotment shall be made pro rata in relation to the number of units the subscriber in total has applied for subscription of units; and thirdly, to those who have provided underwriting commitments with regard to subscription of units, in proportion to such underwriting commitments. To the extent that allotment in any section above cannot be done pro rata, allotment shall be determined by drawing of lots.

Change of share capital and number of shares as well as dilution
The Board of Directors will, inter alia, propose to the extraordinary general meeting on 26 January 2024 that the share capital shall be reduced with SEK 37,186,641.12, from SEK 58,104,126.75 to SEK 20,917,485.63. This reduction will mean that the quota value per share is reduced from SEK 0.25 to SEK 0.09.

Upon full subscription in the Rights Issue, the number of shares in the Company will increase by a maximum of 464,833,014 shares from 232,416,507 to 697,249,521 and the share capital will increase by a maximum of SEK 41,834,971.26 from SEK 20,917,485.63 to SEK 62,752,456.89 (calculated on the new quota value following the contemplated share capital decreases proposed by the Board of Directors to the extraordinary general meeting on 26 January 2024). For existing shareholders not participating in the Rights Issue this will entail, upon full subscription, a dilution effect of approximately 66.7 per cent of the votes and capital of the Company.

In the event all warrants series of TO 8 are fully exercised to subscribe for new shares in the Company, the number of shares will increase by an additional 232,416,507 shares to a total of 929,666,028 shares. This corresponds to a dilution from the warrants of an additional maximum of 25.0 per cent.

The total dilution in the event the Rights Issue is exercised in full and all warrants of series TO 8 are fully subscribed and all warrants of series TO 8 are exercised for the subscription of new shares, thus amounts to 75.0 per cent.

Subscription undertakings and guarantee commitments
Chordate Medical has received subscription undertakings from certain existing shareholders as well as members of the Board of Directors and executive management, amounting to a total of approximately SEK 10.7 million, corresponding to approximately 25.7 per cent of the Rights Issue. No remuneration is paid for submitted subscription undertakings. The Company has also entered into agreements with a number of external investors regarding guarantee commitments of a total of approximately SEK 12.3 million, corresponding to approximately 29.3 per cent of the Rights Issue. Cash compensation is paid according to the guarantee agreements of fifteen (15) per cent of the guaranteed amount, corresponding to approximately SEK 1.8 million in total, or twenty (20) per cent of the guaranteed amount in the form of newly issued units in the Company, on the same terms and conditions as in the Rights Issue, however the subscription price per unit shall correspond to the volume weighted average price for the Company’s share on Nasdaq First North Growth Market during the subscription period in the Rights Issue (i.e. 2 February 2024 – 16 February 2024) multiplied by two (2), but never lower than the subscription price in the Rights Issue or the quota value of the shares multiplied by two (2).

In aggregate, the Rights Issue is covered by subscription undertakings and guarantee commitments of approximately SEK 23.0 million, corresponding to approximately 55.0 per cent of the Rights Issue.

In order to enable issue of units as guarantee remuneration to the guarantors who choose to receive guarantee remuneration in the form of newly issued units, the Board of Directors has proposed that the extraordinary general meeting on 26 January 2024, which, among other things, is proposed to resolve on the approval of the Rights Issue, reductions of the share capital and amendment of the articles of association, also resolves to authorize the Board of Directors to resolve on the issue of such units to the guarantors.

Lock-up undertakings
In connection with the Rights Issue, all board members and senior executives with shareholdings in Chordate Medical have undertaken towards Vator Securities AB, with customary exceptions, not to sell or carry out other transactions with the same effect as a sale without, in each individual case, first having obtained a written approval from Vator Securities AB. The decision to give such written consent is decided by Vator Securities AB and an assessment is made in each individual case. Granted consent can depend on both individual and business reasons. The lock-up undertakings only apply to the shares that are held before the Rights Issue and the lock-up period lasts 180 days after the announcement of the Rights Issue.

Preliminary timetable for the Rights Issue

26 January 2024 Extraordinary general meeting
29 January 2024 Estimated day for publication of prospectus
29 January 2024 Last day of trading including the right to receive unit rights
30 January 2024 First day of trading excluding the right to receive unit rights
31 January 2024 Record date for participation in the Rights Issue
2 February – 13 February 2024 Trading in unit rights on Nasdaq First North Growth Market
2 Feburary – 16 February 2024 Subscription period
2 February 2024 – Until the Rights Issue is registered by the Swedish Companies Registration Office Trading in paid subscribed units (Sw. “BTU”)
Around 20 February 2024 Publication of outcome in the Rights Issue

Extraordinary general meeting
The Board of Directors’ resolution on the Rights Issue is subject to approval by the extraordinary general meeting on 26 January 2024. The resolution on the Rights Issue is subject to and conditional upon that the extraordinary general meeting also resolves to reduce the share capital and to amend the articles of association in accordance with the Board of Directors’ proposal to the extraordinary general meeting. Notice to the extraordinary general meeting will be published through a separate press release.

Prospectus
Full terms and conditions and instructions for the Rights Issue as well as other information about the Company will be presented in the prospectus that the Company expects to publish around 29 January 2024 (the "Prospectus").

Advisers
Vator Securities acts as financial adviser and Wistrand Advokatbyrå acts as legal adviser to the Company in connection with the Rights Issue. Vator Securities also acts as issuer agent in connection with the Rights Issue.

Year-end report for 2023
Due to the Rights Issue, the Board of Directors of Chordate Medical has resolved to postpone the publication of the year-end report for 2023, from 29 February 2024 to 22 March 2024.

IMPORTANT INFORMATION
The information in this press release does not contain or constitute an offer to acquire, subscribe or otherwise trade in shares, warrants or other securities in Chordate Medical. No action has been taken and measures will not be taken to permit a public offering in any jurisdictions other than Sweden. Any invitation to the persons concerned to subscribe for units in Chordate Medical will only be made through the Prospectus that Chordate Medical estimates to publish on or around 29 January 2024 on Chordate Medical’s website, www.chordate.com. The upcoming approval of the Prospectus by the Swedish Financial Supervisory Authority shall not be regarded as an approval of the Company’s shares, warrants or any other securities. This release is not a prospectus in accordance with the definition in the Prospectus Regulation (EU) 2017/1129 (“Prospectus Regulation”) and has not need approved by any regulatory authority in any jurisdiction. This announcement does not identify or suggest, or purport to identify or suggest, the risks (direct or indirect) that may be associated with an investment in shares, warrants or other securities in Chordate Medical. In order for investors to fully understand the potential risks and benefits associated with a decision to participate in the Rights Issue, any investment decision should only be made based on the information in the Prospectus. Thus, investors are encouraged to review the Prospectus in its entirety.

The information in this press release may not be released, distributed or published, directly or indirectly, in or into the United States of America, Australia, Belarus, Canada, Hong Kong, Japan, New Zealand, Russia, Singapore, South Africa, South Korea, Switzerland or any other jurisdiction in which such action would be unlawful or would require registration or any other measures than those required by Swedish law. Actions in violation of these restrictions may constitute a violation of applicable securities laws. No shares, warrants or other securities in Chordate Medical have been registered, and no shares, warrants or other securities will be registered, under the United States Securities Act of 1933, as amended (the “Securities Act”) or the securities legislation of any state or other jurisdiction in the United States of America and no shares or other securities may be offered, sold or otherwise transferred, directly or indirectly, in or into the United States of America, except under an available exemption from, or in a transaction not subject to, the registration requirements under the Securities Act and in compliance with the securities legislation in the relevant state or any other jurisdiction of the United States of America.

Within the European Economic Area (“EEA”), no public offering of shares, warrants or other securities (“Securities”) is made in other countries than Sweden. In other member states of the EU, such an offering of Securities may only be made in accordance with the Prospectus Regulation. In other member states of the EEA which have implemented the Prospectus Regulation in its national legislation, any offer of Securities may only be made in accordance with an applicable exemption in the Prospectus Regulation and/or in accordance with an applicable exemption under a relevant national implementation measure. In other member states of the EEA which have not implemented the Prospectus Regulation in its national legislation, any offer of Securities may only be made in accordance with an applicable exemption under national law.

In the United Kingdom, this document and any other materials in relation to the securities described herein is only being distributed to, and is only directed at, and any investment or investment activity to which this document relates is available only to, and will be engaged in only with, “qualified investors” (within the meaning of the United Kingdom version of the EU Prospectus Regulation (2017/1129/ EU) which is part of United Kingdom law by virtue of the European Union (Withdrawal) Act 2018) who are (i) persons having professional experience in matters relating to investments who fall within the definition of “investment professionals” in Article 19(5) of the Financial Services and Markets Act 2000 (Financial Promotion) Order 2005 (the “Order”); (ii) high net worth entities etc. falling within Article 49(2)(a) to (d) of the Order; or (iii) such other persons to whom such investment or investment activity may lawfully be made available under the Order (all such persons together being referred to as “relevant persons”). In the United Kingdom, any investment or investment activity to which this communication relates is available only to, and will be engaged in only with, relevant persons. Persons who are not relevant persons should not take any action on the basis of this press release and should not act or rely on it.

This press release may contain forward-looking statements which reflect the Company’s current view on future events and financial and operational development. Words such as “intend”, “will”, “expect”, “anticipate”, “may”, “believe”, “plan”, “estimate” and other expressions which imply indications or predictions of future development or trends, and which are not based on historical facts, are intended to identify forward-looking statements. Forward-looking statements inherently involve both known and unknown risks and uncertainties as they depend on future events and circumstances. Forward-looking statements do not guarantee future results or development and the actual outcome could differ materially from the forward-looking statements.

This information, the opinions and the forward-looking statements included in this press release are only applicable as of this date and may change without any notice thereof. Chordate Medical does not undertake to publish any updates or amendments of forward-looking statements, future events or similar circumstances other than what is required by appliable legislation.

First patients included in Chordate Medical’s Post-Market Study PM010

Chordate Medical Holding AB (publ) (“Chordate”) announces today that the first seven patients have been included in the company’s post-Market Study PM010. The seven patients have been enrolled by the study at neurology clinics in Hull, Glasgow, Frankfurt, Essen, and Jerusalem.

“All participating clinics are led by reputable specialists, and it is satisfying that the first patients are now enrolled. The PM010 study is part of the regulatory requirement for the CE marking of migraine treatment but also holds significant importance in providing information to treating physicians about how often the treatment needs to be administered to different types of patients”, says Anders Weilandt, CEO of Chordate.

About PM010
The PM010 study is an ongoing, open post-marketing clinical follow-up investigation to follow long-term performance and safety of Chordate Medical’s preventive migraine treatment Ozilia® in subjects with chronic migraine during regular clinical treatment. The study will recruit 200 subjects and will be conducted at approximately 15 clinics in four European countries, the follow-up is 12 months. Data from this open study will be reported in intervals and used to fine-tune recommendations for the clinical treatment regime.

Record Attendance for Chordate Medical at Congress – “High Buying Interest from Several Markets”

Chordate Medical's CEO Anders Weilandt and CSO Jan Hermansson are currently in Barcelona at the European Headache Congress to present Ozilia to the gathered migraine and headache industry. The congress is attended by 2,200 delegates from both Europe and other markets, and the interest in Ozilia is continuing to grow.

"During the first days, we have generated an impressive number of leads from stakeholders who clearly indicate buying interest. Awareness of Ozilia is beginning to establish itself at very satisfactory levels. We cannot currently serve all interested stakeholders since some markets outside the EU and GCC require product registration – but the need for Ozilia as a drug-free treatment alternative for migraine is evident," says Anders Weilandt.

Chordate is in Barcelona together with the company's Italian distributor Vedise Hospital S.p.A, who will bring home a number of leads. EHC is one of the foremost meeting places for the headache and migraine sector, with representatives from both research and industry from around the world.

"In addition to significant interest from the healthcare sector, we also notice that the exploratory interest from the pharmaceutical industry has increased significantly compared to previous congresses where we have participated. It is evident that they both want to learn more and understand what we are doing."

First patient included in Chordate Medical’s pilot study PM009

Chordate Medical Holding AB (publ) ("Chordate") announced today that the first patient has been included in the company's open pilot study PM009. The study aims to evaluate the effectiveness of Ozilia in the preventive treatment of patients with chronic migraine who do not respond to treatment with CGRP inhibitors and other migraine medications.

“PM009 is an important study with significant potential upside for the company. Every level of positive results from the study could represent a great opportunity for the company, as the patient group in question has very few treatment options left”, says Anders Weilandt, Chordate CEO.

PM009 is being conducted at King's College in London with three to four referring clinics and Dr. Jan Hoffmann as the responsible principal investigator. The goal is to include 25–30 patients in the study.

“PM009 is a pilot study where we can learn more about how Ozilia can help people with chronic migraine who have no other options left. The patients participating in the study have already tried at least three other preventive medications before being treated with CGRP inhibitors, and when they also do not respond to CGRP, there are not many more possibilities. Hopefully, Ozilia can have a positive effect for some of them”, says Jan Hermansson, Chordate CSO.

Chordate’s CEO on client visits in the Gulf region: ”A growing market with great potential for Ozilia”

Chordate Medical's CEO, Anders Weilandt, recently returned from Saudi Arabia and the United Arab Emirates, where he met with both existing and potential clients, and signed an agreement with a new marketing agent for the UAE.

"It has been a rewarding week where, together with our General Manager for GCC, Alain Durante, and Janin Medical, we met several healthcare organizations interested in Ozilia. We also visited IMC International Medical Center Jeddah, which has been treating rhinitis with Ozilia for a long time, and Nadicare Clinics with now six sites around Jeddah, which recently started using Ozilia on the first clinic," says Anders Weilandt.

The Gulf region has long been one of Chordate's priority markets to demonstrate proof of concept, and Ozilia has been used by several private hospitals for the treatment of rhinitis for an extended period.

"It is clear that the demand for treatments like Ozilia is significant in the region, and after the gradual establishment of the rhinitis treatment in the market, the next step is to launch Ozilia for chronic migraine and simultaneously bring in more clients on the rhinitis side," says Anders Weilandt.

Chordate Medical launches Ozilia migraine and rhinitis treatment in the United Arab Emirates

Chordate Medical ("Chordate," "the company") has contracted MEDSWAN MEDICAL SUPPLIES L.L.C, Dubai, as a market expert in the United Arab Emirates (UAE) for the introduction of the company's product Ozilia to the UAE market. As previously announced, the company intends to explore opportunities in the broader Gulf region based on the successes and experiences gained in Saudi Arabia, making the move into the UAE market a logical next step.

Medswan is owned and led by Hanna Hardwick, a Swedish Arabic-speaking businesswoman with 20 years of experience in leading sales and marketing positions within the medtech and pharma sectors in the MEA region. She has worked for global companies such as Sirtex, Terumo, Fresenius, Hilrom, and Siemens.

"Based on several important customer contacts for the UAE that we have collected at recent international congresses, we are expanding our focus primarily on chronic migraine in the Gulf region. Medswan will now register the products, a process estimated to take ten weeks, and concurrently launch and create market access for Ozilia. Hanna Hardwick has extensive experience in relevant specialist segments within medtech, a strong familiarity with market introductions, and a broad network," says Anders Weilandt, CEO of Chordate.

"The healthcare market in the UAE is almost entirely private and relatively straightforward to access. In recent days, we have visited four leading neurologists at as many hospitals here in Dubai – there is no doubt that Ozilia is a drug-free alternative that doctors here see a significant need to have access to."

Chordate Medical receives its first installation of the Ozilia migraine treatment at a private clinic in Hamburg

Chordate Medical has secured an agreement for the immediate installation of equipment and consumables for the Ozilia treatment for chronic migraines. The agreement was reached through the company's marketing consultants in Germany. The customer is a private specialist clinic in Hamburg.

“It is very satisfying to achieve a breakthrough in Germany as it is one of the markets we are focusing on. This will undoubtedly make it easier to continue converting prospects into orders in Germany. The agreement came about thanks to the skilled work of our German market experts,” says Anders Weilandt, CEO of Chordate.
 
Chronic migraines in Germany
Migraine is one of the most common diseases globally, with approximately 12.5 million people in Germany suffering from migraines in some form. That's about one in seven Germans. Globally, it affects around 1.2 billion people. Between 1.5 and 1.8 million Germans have chronic migraines. Migraine and headache care in the country are among the most advanced in Europe, and the market for migraine medications is one of the largest in the world. These conditions where part of the reason why Chordate conducted its recently concluded clinical study in Germany.

The post-market study of Chordate’s Ozilia® migraine treatment has commenced in four different markets

The clinical post-market study, PM010, for Chordate's migraine treatment Ozilia® (formerly K.O.S) has started. The study is designed for 200 patients across up to 15 clinics in the United Kingdom, Germany, Italy, and Israel. It is an open observational study with a 12-month follow-up.

Post-Market Surveillance, a part of the regulatory requirements for the CE marking of the migraine product, is crucial for providing information to treating physicians on how often the treatment needs to be administered to different types of patients.

The first clinic to start is Hull University Teaching Hospitals NHS Trust in Hull, UK, where Professor Fayyaz Ahmed is the investigator in the study, which has begun recruiting approximately 10 patients. Ethical approvals and agreements with other clinics and countries are in place.

"It is satisfying that we are now underway with PM010 after hard work in selecting the right clinics and managing ethics and study agreements in each region where the study will be conducted. It has been important to involve clinics with a relatively large patient flow, focusing on normal clinical operations rather than study-related activities," says Jan Hermansson, Medical Director at Chordate.

Chordate Medical's Ozilia® (formerly K.O.S) migraine treatment is a new and alternative method for chronic migraine. Ozilia® has been CE-marked since May 2021 for the preventive treatment of chronic migraine in adults over 18 years old and is marketed in selected European markets and Israel.

Read more about the completed, ongoing, and planned studies on the Ozilia® treatment

Chordate Medical Holding (publ) Interim Report July-September 2023

Summary of the period July–September 2023

  • Net turnover was SEK 210,947 (0)
  • Cash flow from operating activities was SEK -4,961,395 (-5,623,481)
  • Profit/loss after financial items was SEK -4,938,361 (-6,139,836)
  • Profit/loss after tax was SEK -4,938,361 (-6,139,836)
  • Earnings per share were SEK -0.02 (-0.04)

Summary of the period January–September 2023

  • Net turnover was SEK 494,684 (88,170)
  • Cash flow from operating activities was SEK -19,761,647 (-18,852,271)
  • Profit/loss after financial items was SEK -19,343,762 (-19,481,497)
  • Profit/loss after tax was SEK -19,343,762 (-19,481,497)
  • Earnings per share were SEK -0.08 (-0.12)

INTERNATIONAL INTEREST AND NEW BRAND NAME
The third year of the quarter marked the start of the fall’s series of scientific congresses where we also launched the new brand name Ozilia® that now replaces K.O.S on all markets where the treatment is offered. The period started with a poster presentation at the International Headache Congress in Seoul of the results from our crucial migraine study PM007. Ozilia® was mentioned by several other lecturers as a potentially valuable alternative when medication is not appropriate or desirable.

  • Study results presented at IHC2023 in Seoul
  • Submission of article manuscript for PM007
  • Presentation in Berlin of case study from the migraine study
  • Launch of new brand name Ozilia®
  • New commission analysis

Study results presented at IHC2023 in Seoul
After the first presentations in Austin and Berlin in July, the clinical study results from PM007 were also presented to basically the global leaders in migraine care, research and the industry at the International Headache Congress in Seoul September 14–17. This was the first time Chordate exhibited at an international level, which clearly indicated that Ozilia® is viewed as a relevant medicine-free alternative and knowledge about our treatment technique was properly disseminated among key congress participants. We were able to connect with valuable new contacts in both Europe and the USA that have the potential to lead the development of our business in an interesting direction.

Presentation in Berlin of case study from the migraine study
Dr. Tim Jürgens presented a case study from the migraine study PM007 at The German Migraine and Headache Society congress on June 30 in Berlin. The case study described one of the patients in the study with a headache that was very difficult to treat. After treatment with Ozilia®, the patient showed a sharp reduction in the number of migraine episodes, from 18 to 8 days. The positive effect lasted for four months without further treatment sessions. This is a single case with a remarkable effect. Given that the patient had few functional medical alternatives due to other illnesses, the report shows the value of Ozilia® as an alternative when other existing treatments are ineffective.

Article submitted for PM007
The authors of the PM007 study announced that they had submitted a manuscript to a prominent scientific journal at the end of August. After publication, the article will be a valuable tool in our marketing and sales effort. Published results are also a necessary basis for success in various reimbursement processes.

Launch of new brand name Ozilia®
Our treatment is now marketed under the name Ozilia® or Ozilia® Migraine. The new brand name is the next step in the rollout and commercialization of the treatment on our key markets. The name has been warmly received, with special attention given to the fact that it is a female name since around 70 percent of migraine patients are women.

New commission analysis
Of more than 900 listed companies in Sweden, it is estimated that one-third offer so-called commission analyses to facilitate the assessment of the company for its owners and stakeholders. Chordate is now ordering a commission analysis from Kalqyl for the same reason. We are taking steps toward the long-term goal of being able to offer our owners a bid from an international actor who is interested in adding our technology to their product portfolio. The value of the company should then theoretically be the same as the value that the buyer sees in marketing and selling the technology where it is active, often globally. We assume in principle that such hypothetical bids reasonably should constitute part of the theoretical value for the technology, but not all of it. Traditional equity or corporate analysis is often based on present value calculations of unrestricted cash flow; in other words, the value in the new few years of the profit that a business can generate itself that is not needed for some other activity in the business. The analysis principle, which is the most common and in most cases the proper tool, becomes problematic when the strategy in the company that is being analyzed instead is about showing a value in a buyer’s assessment—where the technology can have a much larger value for another party than what the company itself can achieve through profit generation from its own sales. We have therefore signed an agreement for a commissioned analysis from Kalqyl, which we, like most other small companies, will pay for. Kalqyl and other analysis firms conduct and publish their analyses at their own risk and independent from the client to preserve their reputation, which for them is crucial for their existence. We make the assessment that Kalqyl has the capacity and interest to perform a strategy-based analysis and publish it as part of the basis for the market’s assessment of Chordate.

Focus during the rest of the year
During the last part of the year, work will continue in our focus markets Finland, Germany, the UK, Italy, (Israel, unfortunately temporarily halted) and Saudi Arabia. The list of prospective clients is growing, and we are approaching our targets on several points. Marketing is in the form of exhibitions at specialist congresses:

  • IHC2023, Seoul, South Korea, 9/14–17
  • Deutscher Schmerzkongress 2023, Mannheim, 10/18–21
  • Neurologdagarna 2023, Helsinki, Finland, 11/1–3
  • EHC2023, Barcelona, 12/6–9

Kista, October 2023
Anders Weilandt, CEO

Chordate Medical presents interim report for Q3 2023 on Finwire TV

Chordate Medical Holding (publ) is releasing its interim report for Q3 2023 on Wednesday, November 1st, at 08:30. On the same day, at 10:00, the company invites you to a webcast presentation of the report with CEO Anders Weilandt on Finwire TV.

The presentation can be viewed through the following link: https://www.finwire.tv/webcast/chordate-medical/q3-2023/

Following the presentation, there will be a Q&A session where viewers can submit questions.

A recording of the presentation will be made available afterwards on the company’s website www.chordate.com and on Finwire TV’s YouTube channel.