Fredag 2 Oktober | 00:01:26 Europe / Stockholm
Est. tid*
2027-04-20 N/A Årsstämma
2027-02-25 08:30 Bokslutskommuniké 2026
2026-08-27 - Kvartalsrapport 2026-Q2
2026-05-19 - Årsstämma
2026-04-23 - X-dag ordinarie utdelning PILA 0.00 SEK
2026-02-26 - Bokslutskommuniké 2025
2025-08-27 - Kvartalsrapport 2025-Q2
2025-04-30 - X-dag ordinarie utdelning PILA 0.00 SEK
2025-04-29 - Årsstämma
2025-02-27 - Bokslutskommuniké 2024
2024-08-27 - Kvartalsrapport 2024-Q2
2024-05-17 - X-dag ordinarie utdelning PILA 0.00 SEK
2024-02-28 - Bokslutskommuniké 2023
2023-10-25 - 15-10 2023-Q3
2023-08-23 - Kvartalsrapport 2023-Q2
2023-05-31 - X-dag ordinarie utdelning PILA 0.00 SEK
2023-05-30 - Årsstämma
2023-02-28 - Bokslutskommuniké 2022
2022-10-26 - Kvartalsrapport 2022-Q3
2022-08-26 - Kvartalsrapport 2022-Q2
2022-06-08 - X-dag ordinarie utdelning PILA 0.00 SEK
2022-06-07 - Årsstämma
2022-04-26 - Kvartalsrapport 2022-Q1
2022-02-18 - Bokslutskommuniké 2021
LandSverige
ListaFirst North Stockholm
SektorHälsovård
IndustriBioteknik
PILA PHARMA är ett kliniskt bioteknikbolag baserat i Malmö, Sverige. Bolaget utvecklar nya orala läkemedel för globalt vanliga metabola sjukdomar som diabetes, fetma och hjärt-kärlsjukdomar samt terapier för smärtbehandling. Bolaget har erhållit en särläkemedelsbeteckning i USA för den sällsynta sjukdomen Erythromelalgia. Bolaget är specialiserat på utveckling av farmaceutiska läkemedel baserade på TRPV1-antagonister.

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PILA PHARMA: FIRST SUBJECT FIRST VISIT COMPLETED FOR SAFETY PART 1 OF PP-CT04, A CLINICAL TRIAL IN PEOPLE LIVING WITH OBESITY

2026-09-30 17:15:00

30 September 2026, Malmö Sweden: PILA PHARMA AB (publ) (FN STO: PILA)(FRA:5KC), a clinical stage biotech company pioneering development of an oral TRPV1-antagonist as a potential first-in-class treatment for obesity and diabetes, today announces that the first subject first visit (FSFV) for the Part 1 (safety) of PP-CT04 has been enrolled. In total 6 subjects were screened on the first day.


PP-CT04 is a two-part, randomised, double-blind, placebo-controlled, parallel-group, 12‑week trial investigating the safety, tolerability, pharmacokinetics and efficacy of XEN-D0501 in obese participants.

The trial is designed to explore a within-subject dose titration approach to reach anticipated therapeutic plasma concentrations of XEN-D0501 not previously investigated.

Dose escalation will be carried out individually for each participant, beginning at 4 mg BID and increasing stepwise up to a maximum of 16 mg BID. Each dose level will be administered for 1 week, resulting in a maximum dose escalation period of 4 weeks. Once the highest tolerable dose has been reached and confirmed to be tolerable, the participant will continue treatment at that dose for an 8-week maintenance period.

PP-CT04 is divided into two parts with the same overall design, but Part 1, as a pilot safety cohort with 8 participants, entails more intense safety monitoring. This is done in collaboration with Clinical Trial Consultants AB.

Part 2 may start once all participants in Part 1 have been dosed for at least 5 weeks and once a favourable recommendation has been given by the internal safety review committee.

For more information:

Gustav H. Gram, CEO

ghg@pilapharma.com

PILA PHARMA’s share ticker PILA is subject to trade on Nasdaq First North Growth Market, Sweden with Aqurat Fondkommission AB as Certified Adviser.
Contact: M: ca@aqurat.se -
T: +46 (0)8 684 05 800



About PILA PHARMA AB (Publ)

PILA PHARMA AB is a Swedish clinical stage biotech company based in Malmö, Sweden. The aim of the company is to develop TRPV1 antagonists as a novel treatment of obesity and diabetes. The Company owns a TRPV1 asset with data and chemical entities including the clinical development candidate XEN-D0501. In July 2022, the Company was moreover awarded orphan drug designation ("ODD") for XEN-D0501 as a treatment for the painful rare disease erythromelalgia.