Uppsala,
NOT FOR RELEASE, DISTRIBUTION OR PUBLICATION, DIRECTLY OR INDIRECTLY, IN OR INTO,
Summary
- In light of Dicot's consistently good results to date, the Board of Directors considers that it is in the shareholders' interest to reserve the right for the current owners to be able to benefit from the future value-creating development and thus seek external capital at a later date. The work of establishing partnerships will continue in parallel with the further development of the Company's assets.
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The Board of Directors in Dicot therefore announces its intention to resolve on a Rights Issue amounting to approximately
SEK 125 million before deductions for transaction costs. In addition, the Company can receive additional proceeds from the warrants issued as part of the Units.
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The purpose of the Rights Issue is primely to finance a clinical phase 2a trial. The Company also intends to start preparations for a clinical phase 2b trial in parallel.
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An EGM in the Company is proposed to resolve on an authorization for the Board of Directors to resolve on the Rights Issue. The EGM is planned to be held on
August 1, 2024 , and the notice will be published through a separate press release.
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The Rights Issue and its full terms are subsequently expected to be resolved by the Board of Directors around
August 7, 2024 , based on the authorization. The Rights Issue is covered to approximately 65.0 percent through a combination of subscription commitments and underwriting undertakings. Provided that the EGM grants the Board of Directors an authorization to resolve on the Rights Issue and the Board of Directors resolves on the Rights Issue:-
certain existing shareholders, the founder of the Company, and all members of the Board of Directors and executive management have undertaken to subscribe for Units in the Rights Issue. All have committed to vote in favor of the authorization for the Board of Directors at the EGM. Total subscription commitments amount to approximately
SEK 17.5 million , equivalent to approximately 14.0 percent of the Rights Issue; and -
a few external investors have provided underwriting undertakings subject to customary conditions which, in aggregate, amount to approximately
SEK 63.8 million , equivalent to approximately 51.0 percent of the Rights Issue.
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certain existing shareholders, the founder of the Company, and all members of the Board of Directors and executive management have undertaken to subscribe for Units in the Rights Issue. All have committed to vote in favor of the authorization for the Board of Directors at the EGM. Total subscription commitments amount to approximately
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The Company's Shareholders on the record date will receive unit rights that give the right to subscribe for Units, which will consist of shares and warrants that give the holder possibility of additional subscription of shares at a later date. It is expected that the Units will be structured with a 4:1 ratio of shares and warrants where, for example, for every four shares, a warrant will be included in a Unit.
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The subscription price when subscribing additional shares through the exercise of warrants obtained when subscribing to Units will be within the range of 100 and 150 percent of the subscription price in the Rights Issue.
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The subscription price when subscribing additional shares through the exercise of warrants obtained when subscribing to Units will be within the range of 100 and 150 percent of the subscription price in the Rights Issue.
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The Rights Issue, including full terms, inter alia, subscription price, number of new shares issued and increase of the share capital, with the support of the authorization, is expected to be resolved by the Board of Directors around
August 7, 2024 . The subscription price will be priced at a customary discount to the theoretical ex-rights price ("TERP").
Background and reasons
Dicot Pharma is developing the drug candidate LIB-01 to treat erectile dysfunction and premature ejaculation in men, which is common worldwide. Studies show that more than half of all men over 40 suffer from erectile dysfunction to some degree. The most used potency drugs today have certain drawbacks and almost half of all those who try these drugs choose to discontinue the treatment. Around 35 percent do not get the desired effect and many experience side effects and concerns about cardiovascular effect. Medications like Viagra also have a short duration of action and require planning, which reduces the spontaneity of sex life.
The Company's goal with LIB-01 is to create a completely new generation of potency drugs that surpass current available treatments; with longer duration of action, fewer side effects and a differentiated mode if action. A treatment where the effect lasts for a long time would be equal to great advantages. Affected men do not have to plan their sex life, which results in a more normal everyday life and increases the quality of life. "LIB-01, with its unique duration of action, promises a paradigm shift in the treatment of erectile dysfunction. It is the first revolutionary molecule to come into the field since Viagra", comments the world's leading medical expert in erectile dysfunction, Dr
Dicot has taken important steps in the development of LIB-01. In 2024, the Company completed its phase 1 clinical trial with very positive results showing that LIB-01 has a good safety profile. In addition to this, an efficacy signal could be where participants reported an improved erectile function, in some cases beyond 28 days post first dose. In parallel with this, the Company has made significant preparations for an upcoming clinical phase 2a trial such as completed GMP manufacturing of the study drug. The Company intends to start a clinical phase 2a trial during the fourth quarter of 2024.
The Company is now planning for a rights issue of Units with the aim of conducting a clinical phase 2a trial. The Company also intends to start preparations for clinical phase 2b studies in parallel. This follows the Company's business strategy to develop LIB-01 under its own auspice until phase 2a trial. Dicot's ambition is to enter into collaborations with other established pharmaceutical companies ahead of future clinical phases to finance, further develop and launch LIB-01 on the world market.
The issue proceeds after deducting issue costs are intended to finance the following activities:
- Implementation of the clinical phase 2a study, as well as preparations for the clinical phase 2b study.
- Other R&D and scaling up of the manufacturing process.
- Preclinical studies for the development of new indications.
- Business development, patents, quality and regulatory processes, etc.
- Corporate governance and management (incl. legal, IT, insurance, marketplace, personnel, board, etc.)
Extraordinary general meeting and expected timetable for the Rights Issue
An EGM is proposed to authorize the Board of Directors to resolve on the Rights Issue. The EGM is planned to be held in Uppsala on
Subscription commitments, underwriting undertakings and voting commitments
Provided that the EGM authorizes the Board of Directors to resolve on the Rights Issue and the Board of Directors subsequently resolves to carry out the Rights Issue, certain existing shareholders, among others
A few external investors have provided underwriting undertakings subject to customary conditions, which in aggregate, amount to approximately
Neither of these commitments are secured by bank guarantee, blocked funds, pledges or similar arrangements. Further information regarding the parties who have submitted subscription commitments and underwriting undertakings will be stated in the prospectus published before the start of the subscription period.
Earlier publication of interim report
As a result of the Rights Issue, the Company has resolved to bring forward the date of publication of the interim report for the second quarter of 2024 to
Prospectus
Complete information and instructions regarding the Rights Issue and other information about the Company will be provided in the prospectus which will be published before the start of the subscription period. The prospectus and subscription form will be made available on Dicot's website www.dicotpharma.com as well as on
Advisors
For further information, please contact:
Phone: +46 72 502 10 10
E-mail: elin.trampe@dicotpharma.com
About
Dicot Pharma is developing the drug candidate LIB-01, which will be a potency agent to better treat erectile dysfunction and premature ejaculation. The ambition is to create a drug with significantly longer effect and far fewer side effects, compared to current available drugs. Today, over 500 million men suffer from these sexual dysfunctions and the market is valued at
Dicot is listed on
Important Information
The information in this press release neither contains nor constitutes an offer to acquire, subscribe or otherwise trade in shares, warrants or other securities in Dicot. No action has been taken and no action will be taken to permit an offer to the public in any jurisdictions other than
The information contained in this press release may not be disclosed, published or distributed, directly or indirectly, within or to
This press release is not a prospectus within the meaning of Regulation (EU) 2017/1129 (the "Prospectus Regulation") and has not been approved by any regulatory authority in any jurisdiction. In an EEA Member State, other than
In the
Forward-looking statements
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", "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.
The English text is an unofficial translation of the original Swedish text. In case of any discrepancies between the Swedish text and the English translation, the Swedish text shall prevail.
This disclosure contains information that
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