By mistake a draft version of the press release was published at 08:30 today, where the business highlights and the relevant period had not been updated. This has now been corrected.

Business highlights in Q3 2025

  • In July the Company announced the outcome of the Company’s rights issue of up to 14,039,590 shares (the “Rights Issue”), for which the subscription period ended on 26 June 2025. In the Rights Issue, 6,133,159 shares, corresponding to around 43.7 percent of the Rights Issue were subscribed through subscription rights. Additionally, 277,458 shares, corresponding to around 2.0 percent of the Rights Issue were subscribed without subscription rights. 5,670,164 shares, corresponding to around 40.4 percent of the Rights Issue were subscribed through guarantee undertakings. The Rights Issue will provide the Company with proceeds of approximately SEK 48.3 million before deduction of costs related to the Rights Issue.
  • In September the Company announced the submission of a clinical trial application (CTA) to the UK’s Medicines and Healthcare products Regulatory Agency (MHRA), and local ethics committee in the UK for the approval to conduct a Phase IIa clinical proof-of-concept study in women suffering from vulvodynia, a severe chronic pain condition affecting approximately 10 percent of women worldwide. The study will be conducted together with MAC Clinical Research in the UK.

Business highlights after this reporting period

  • In November the Company announced that its Clinical Trial Application (CTA) for the planned Phase IIa clinical proof-of-concept study in women with vulvodynia has been approved by the UK Medicines and Healthcare products Regulatory Agency (MHRA) and a local ethics committee. First patients are expected to be enrolled in Q4 2025.

Financial Highlights

Third Quarter (2025-07-01 – 2025-09-30)
Net revenue were KDKK 0 (0)
Operating loss, EBIT was KDKK -4,318 (-3,233)
Earnings per share before and after dilution was DKK -0.06 (-0.06)
Cash: KDKK 28,674 (11,979)
Solidity: 88% (92%)

First Nine Months (2025-01-01 – 2025-09-30)
Net revenues were TDKK 0 (0)
Operating loss, EBIT was TDKK -10,815 (-11,801)
Earnings per share before and after dilution was DKK –0.16 (-0.22)

Solidity: equity divided by assets.

The Board of Directors have decided that interim reports will be published in English only.

Link to the full report
https://www.initiatorpharma.com/en/investors/reports-and-presentations/

For additional information about Initiator Pharma, please contact:

Claus Elsborg Olesen, CEO
Telephone: +45 6126 0035
E-mail: ceo@initiatorpharma.com

About Initiator Pharma

Initiator Pharma A/S is a Danish clinical stage emerging pharma company developing innovative drugs that target key unmet medical needs within the central and peripheral nervous system. Initiator Pharma’s pipeline consists of two clinical stage assets – pudafensine and IP2018 – and one preclinical asset. With pudafensine the company has reported positive, statistically significant and clinically relevant efficacy data in a Phase IIb clinical trial with patients suffering from ED. With IP2018 the company has reported positive, statistically significant, and dose-dependent clinical observations related to efficacy in psychogenic erectile dysfunction (ED) in a Phase IIa clinical trial of IP2018 in patients with mild to moderate ED.

Initiator Pharma is listed on Nasdaq First North Growth Market (ticker: INIT). Redeye AB is the company’s Certified Adviser. For more information, please visit www.initiatorpharma.com.

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2025 Q3 Final

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