
We are pleased to inform that during the summer, the application to start clinical studies of PN6047 was approved by the Swedish Medical Products Agency and Ethical Review Authority. On Monday, the first dose was given to humans.
The primary goal of phase I studies is to investigate the safety and tolerability of thecandidate PN6047. The trials are being carried out by Clinical Trial Consultants AB (CTC, based in Uppsala, Sweden) and will include about a hundred healthy volunteers.
"We are extremely proud and happy to have achieved a milestone we have worked to reach for a very long time. Our vision is to improve the quality of life for people suffering from chronic pain. Going from pre clinical to clinical development is a significant achievement for everyone involved. I want to take this opportunity to thank and congratulate our team; everyone has worked hardand been totally committed to achieving this", says Per von Mentzer, CEO of PharmNovo.
Earlier this summer, PharmNovo completed a share issue of SEK 67 million led by the investor syndicate Sciety. Karolinska Development AB also participated in the share issue. An additional SEK 6 million was added in a rights issue. The capital will be used to implement the clinical phase I studies, produce the drug substance, and continue the company's development.

We are pleased to inform that during the summer, the application to start clinical studies of PN6047 was approved by the Swedish Medical Products Agency and Ethical Review Authority. On Monday, the first dose was given to humans.
The primary goal of phase I studies is to investigate the safety and tolerability of thecandidate PN6047. The trials are being carried out by Clinical Trial Consultants AB (CTC, based in Uppsala, Sweden) and will include about a hundred healthy volunteers.
"We are extremely proud and happy to have achieved a milestone we have worked to reach for a very long time. Our vision is to improve the quality of life for people suffering from chronic pain. Going from pre clinical to clinical development is a significant achievement for everyone involved. I want to take this opportunity to thank and congratulate our team; everyone has worked hardand been totally committed to achieving this", says Per von Mentzer, CEO of PharmNovo.
Earlier this summer, PharmNovo completed a share issue of SEK 67 million led by the investor syndicate Sciety. Karolinska Development AB also participated in the share issue. An additional SEK 6 million was added in a rights issue. The capital will be used to implement the clinical phase I studies, produce the drug substance, and continue the company's development.

Take the opportunity to listen to Per von Mentzer, CEO, presenting PN6047 at the LSX World Europe congress in Lisbon, March 2026. Learn how PharmNovo is shaping a new approach to pain relief with the goal to prove that powerful pain treatment doesn’t have to come with the cost of addiction. Discover how the company’s lead candidate PN6047, delivers effective pain relief without activating the mu-opioid receptor and avoiding the addiction risks associated with conventional opioids. The Phase II-ready Delta Opioid Receptor Agonist (DORA) with first-in-class potential, PN6047 represents a safer, non-addictive approach targeting a neuropathic pain market that is expected to double until 2033 and reach 13 bEUR.
Read morePharmNovo is pleased to announce that that the company has completed drug product manufacturing for its lead candidate PN6047. This is an important milestone as the company prepares for its upcoming Phase IIa proof-of-concept study in neuropathic pain.
Read moreAs the company prepares for the next phase of clinical development, the new Board composition strengthens our strategic capabilities ahead of Phase II development of our lead candidate, PN6047.
Read more