Lipigon ready to apply for clinical trials after successful completion of preclinical safety studies

This is an English translation of the Swedish original. In case of discrepancies, the Swedish original shall prevail.

Lipigon Pharmaceuticals AB ("Lipigon"), which is developing therapeutics for lipid-related diseases, today announced that the final preclinical safety study with the lipid-lowering drug candidate Lipisense has been successfully completed. Lipisense is thus ready for further development for clinical trials, expected to start during the second quarter of 2022.

The reported final study aimed to investigate the safety and tolerability of Lipisense during one month of multiple dosing and rising dose levels. The results show that Lipisense was well tolerated in high doses and a significant dose-dependent reduction in triglycerides could also be observed. Together with previously produced data, these results will form the basis for determining the optimal dose level in the phase I study.

Lipisense is a drug candidate for the treatment of diseases with abnormal levels of lipids in the blood, primarily triglycerides, and a first-in-class treatment with a unique mechanism of action. Elevated triglyceride levels in the blood are a risk factor present in several diseases. Lipisense has the potential to normalize blood triglyceride levels. The patient population with uncontrolled elevated triglycerides is large and heterogeneous-comprising patients with rare genetic disorders to large patient groups, such as type 2 diabetics.

CEO Stefan K. Nilsson comments:

"With this last study, the preclinical security program has been completed and we have reached an important milestone. It is with great pleasure I can state that all studies have shown good results regarding safety and tolerability. We will shortly apply for authorization for the first clinical trial with Lipisense to the Swedish Medical Products Agency. It will be a phase 1 trial of healthy volunteers and a small group of type 2 diabetics with a focus on safety parameters but also good opportunities to measure blood lipid reductions.

In drug development, it is unusual with a scenario where you already in phase 1 can establish efficacy data on the parameter that forms the basis for future drug approval. This would mean a significant risk minimization and open for early business opportunities. During the autumn and winter, we have observed a great deal of interest in RNA-based drugs along with several significant deals. In summary, Lipigon has now entered an exciting stage where we see several important milestones ahead of us already this year."

About Lipisense

The drug candidate is an RNA therapeutics that prevents the cells from producing the disease-promoting target protein ANGPTL4 by destroying the protein-coding RNA before the target protein has been formed. The target gene has a strong genetic association to plasma lipid levels and related diseases, such as type 2 diabetes and cardiovascular disease.

For more information, please contact:
Stefan K. Nilsson, CEO, Lipigon
Phone: +46 705 78 17 68

This is information that Lipigon Pharmaceuticals AB (publ) 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 09:05 am CET, on 2 February 2022.

About Lipigon

Lipigon develops novel therapeutics for patients with lipid metabolism disorders. The company is based on over 50 years of lipid research at Umeå University, Sweden. Lipigon's initial focus is on orphan drugs and niche indications, but in the long term, the company will have the opportunity to target broader indications in the area, such as diabetes and cardiovascular disease. Lipigon's pipeline includes four active projects: the RNA-drug Lipisense for treatment of hypertriglyceridemia; an RNA-drug for treatment of acute respiratory distress syndrome; a gene therapy treatment for the rare disease lipodystrophy, together with Combigene AB (publ); and a small molecule program for the treatment of dyslipidemia in collaboration with HitGen (Inc).

The company's share (LPGO) is traded on the Nasdaq First North Growth Market. Certified Adviser is G&W Fondkommission, email:, phone: +46 8 503 000 50.


Idag, den 19 maj 2022, hölls extra bolagsstämma i Lipigon Pharmaceuticals AB. Extra bolagsstämman beslutade enligt nedan.


I dag, den 19 maj 2022, hölls årsstämma i Lipigon Pharmaceuticals AB. Nedan följer en sammanfattning av de beslut som fattades. Samtliga beslut fattades med erforderlig majoritet.


Lipigons vd Stefan K. Nilsson ska hålla två presentationer om Lipisense under den prestigefyllda "Late Breaking Session" vid EAS Congress 2022 i Milano. Denna årliga kongress samlar de främsta medicinska experterna och forskarna inom åderförfettning. Vid "Late Breaking Session" presenteras de senaste och mest intressanta nya forskarrönen.


Valberedningen i Lipigon Pharmaceuticals AB ("Lipigon") föreslår att Lars Öhman väljs till ordförande vid årsstämman. Nuvarande styrelseordförande Urban Paulsson har meddelat att han inte ställer upp till omval till ordförandeposten, dock står han till förfogande för omval som styrelseledamot.


Lipigon har erhållit godkännande från Läkemedelsverket att starta klinisk prövning av Lipisense, efter att ha presenterat en tillfredställande säkerhetsprofil i det prekliniska arbetet. Analysguiden sätter ett motiverat värde om 11,6 (12,6) kronor på Lipigon.


Lipigon Pharmaceuticals AB ("Lipigon") meddelar i dag att vd Stefan K. Nilsson har köpt aktier i Lipigon till ett sammanlagt värde om 265 tkr till ett genomsnittspris om 3,36 kronor per aktie.


Aktieägarna i Lipigon Pharmaceuticals AB, 556810-9077, ("Bolaget") kallas härmed till extra bolagsstämma den 19 maj 2022 kl. 11.00 i Bolagets lokaler på Tvistevägen 48C i Umeå.


Styrelsen för Lipigon Pharmaceuticals AB (publ) ("Bolaget" eller "Lipigon") har, villkorat av extra bolagstämmas efterföljande godkännande, beslutat om en nyemission av aktier om cirka 25,1 MSEK med företrädesrätt för Lipigons aktieägare ("Företrädesemissionen"). Företrädesemissionen omfattas till 90 procent av tecknings- och garantiåtaganden. Företrädesemissionen är villkorad av att extra bolagsstämma ("Extra Bolagsstämman") godkänner styrelsens beslut.


Lipigon Pharmaceuticals AB ("Lipigon") offentliggör härmed delårsrapport avseende det första kvartalet 2022. Delårsrapporten i sin helhet finns tillgänglig som bifogad fil samt på bolagets hemsida, Nedan följer en kort sammanfattning av delårsrapporten.


Den 30 april 2022 avslutades nyttjandeperioden för Lipigon Pharmaceuticals AB:s ("Lipigon" eller "Bolaget") teckningsoptioner av serie TO1. Inga teckningsoptioner nyttjades.



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