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Regulatory press release

Adjusted timeline for the previously communicated rights issue

AlzeCure Pharma
Download the release

AlzeCure Pharma AB (publ) (FN STO: ALZCUR), a biotech company that develops candidate drugs for diseases affecting the nervous system, focusing on Alzheimer's disease and pain, announces that the timeline for the previously communicated rights issue of approximately SEK 30.1 million is being adjusted due to technical issuance reasons. All terms of the Rights Issue, including the subscription price of SEK 1.31 per share and the issue amount of approximately SEK 30.1 million, remain unchanged.

Updated preliminary timeline:

EventDate
Last day of trading including the right to receive subscription rights10 June 2026
First day of trading excluding the right to receive subscription rights11 June 2026
Record date for participation in the Rights Issue12 June 2026
Trading in subscription rights16 June – 25 June 2026
Subscription period16 June – 30 June 2026
Announcement of the outcome of the Rights IssueAround 2 July 2026

The timeline is preliminary and may be subject to change.

For more information, please contact


Martin Jönsson, CEO
Tel: +46 707 86 94 43
martin.jonsson@alzecurepharma.com

About AlzeCure Pharma AB (publ)


AlzeCure® is a Swedish clinical stage biotech company that develops new innovative drug therapies for the treatment of severe diseases and conditions that affect the central nervous system, such as Alzheimer’s disease and pain – indications for which currently available treatment is very limited. The company is listed on Nasdaq First North Premier Growth Market and is developing several parallel drug candidates based on three research platforms: NeuroRestore®, Alzstatin® and Painless.

NeuroRestore consists of two symptomatic drug candidates where the unique mechanism of action allows for multiple indications, including Alzheimer’s disease, as well as cognitive disorders associated with traumatic brain injury, sleep apnea and Parkinson’s disease. NeuroRestore has received an EU grant from the European Innovation Council and is being prepared for phase 2. Alzstatin focuses on developing disease-modifying and preventive drug candidates for early treatment of Alzheimer’s disease. Painless contains two projects: ACD440, which is a drug candidate for the treatment of neuropathic pain with positive phase 2 results and orphan drug designation from the FDA in the USA and from EMA in Europe for the rare pain disease erythromelalgia, and TrkA-NAM, which targets severe pain in conditions such as osteoarthritis. AlzeCure aims to pursue its own projects through preclinical research and development through an early clinical phase, and is continually working on business development to find suitable outlicensing solutions with other pharmaceutical companies.

FNCA Sweden AB is the company’s Certified Adviser. For more information, please visit www.alzecurepharma.se.

This information is information that AlzeCure Pharma is obliged to make public pursuant to the EU Market Abuse Regulation. The information was submitted for publication, through the agency of the contact persons set out above, at 2026-04-30 08:00 CEST.

Attachments


Adjusted timeline for the previously communicated rights issue