Annexin rights issue 2024
| Published May 20, 2024

Issuance drives Annexin's progress towards Phase II results

Phase II data in the eye disease retinal vein occlusion is approaching for Annexin Pharmaceuticals, which is currently in the process of issuing shares. The company aims to raise SEK 45,1 million, which will primarily finance the completion of the phase IIa study and preparations for the next step in the indication, a phase IIb study. The capital will also cover the company's activities in the cancer area, as well as accelerated business development.

RVO – retinal vein occlusion – is probably one of the lesser-known eye diseases. However, the fact is that the disease is one of the most common causes of vision loss, with more than 16 million patients affected worldwide. Currently, there is no effective treatment that targets the underlying causes of the disease, which is something that Stockholm-based Annexin Pharmaceuticals wants to change things with the drug candidate ANXVThe candidate has also been shown to have potential in the field of cancer.

Potentially revolutionary treatment for RVO

RVO occurs when a vein in the eye becomes blocked by a blood clot, leading to swelling, bleeding and oxygen deprivation in the retina. This results in vision loss, which usually comes on suddenly and can worsen over time. There is currently no cure for RVO. Current options, including the first-line treatment anti-VEGF, are used to treat only its complications, must be repeated many times and are of limited effectiveness. Treatment involves injecting medication directly into the eye over a period of 6 months to several years, and the procedure is experienced by many patients as very uncomfortable.

ANXV is almost identical to the naturally occurring protein Annexin A5. With the candidate, Annexin Pharmaceuticals aims to develop a treatment with a completely new mechanism of action, which could potentially resolve or reduce the blockage in the vein itself that occurs in RVO. ANXV can also reduce inflammation, maintain functioning blood flow and save damaged retinal cells. Instead of being injected directly into the eye, the treatment can also be given intravenously in an arm.

The company is conducting a Proof-of-Concept phase IIa study at eye clinics in the US, which has been closed for recruitment since April. 15 patients are included in the study and so far everything indicates that ANXV has a good safety and tolerability profile. The majority of patients have also shown positive efficacy signals through stable or improved visual acuity and reduced swelling in the eye and the patients have been assessed to need anti-VEGF treatment to a lesser extent than expected, even though a matching control group is missing in the study. Top line data from the study is expected during the summer and Annexin's goal is to subsequently achieve licensing agreements and/or partnerships within the indication.

Exploring ANXV in cancer

The second area that Annexin has chosen to explore is oncology. Independent research shows that Annexin A5's unique properties may be useful in cancer treatment. The company believes that the candidate itself has the potential to affect cancer cells by increasing their susceptibility to immune system attacks. In addition, ANXV can enhance the effect of existing checkpoint inhibitors, which would be valuable since many patients have a suboptimal or absent response to these treatments.

Annexin has also explored the possibility of conjugating – i.e. binding cytotoxic agents to ANXV. This has shown promising results in preclinical studies where the ANXV conjugate was able to effectively kill cancer cells from a patient with triple-negative breast cancer. The company will continue to conduct preclinical and some clinical research to create opportunities for partnerships also in oncology. Read an interview with the CEO Anders Haegerstrand here.

Rights issue drives projects forward

To accelerate the development of the specified projects, Annexin Pharmaceuticals is conducting a rights issue of approximately SEK 28 million until May 2024, 45,1. The largest portion of the issue proceeds, approximately 47 percent, will be used to complete the Phase IIa study and to prepare for Phase IIb studies. The proceeds will also be used for preparatory studies in cancer and business development.

The rights issue is over 90 percent guaranteed through 66 percent of subscription commitments and 25 percent of guarantees from the main owner, board of directors and management.

Summary of the offer

Terms & conditions Each existing share gives one subscription right. Twenty-five subscription rights entitle the holder to subscribe for thirteen new shares.
Subscription period 14 – 28 May 2024
Subscription price SEK 0,25 per share
Volume SEK 45,1 million before issue costs
Pre-money valuation SEK 86,5 million

Prospectus and subscription

Subscription via Avanza

Subscription via Nordnet

Drawing via Hagberg & Aneborn

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