Dicot Pharma’s Phase 2a study completed – results within three months
Prenumeration
Beskrivning
| Land | Sverige |
|---|---|
| Lista | First North Stockholm |
| Sektor | Hälsovård |
| Industri | Läkemedel & Handel |
Uppsala, Sweden, August 20, 2025. Today, potency drug developer Dicot Pharma announces that the clinical part of its phase 2a study has been completed, as the final participant now has completed the last study visit. Results from the study will be reported within three months.
Dicot Pharma had previously communicated that the phase 2a study, evaluating the candidate LIB-01’s effect on erectile function, was expected to be completed in August. Today, the company confirms this as all participants now have completed the final study visit. The next step includes cleaning of collected data, database lock, and subsequent statistical analysis before results can be reported. This process is expected to take two to three months.
“We have just received confirmation that all participants have now completed their visits, marking the completion of the clinical work. Throughout this phase 2a study we have successfully passed each checkpoint in accordance with the original development plan, not least thanks to an excellent effort by our clinical partner CTC. We are now very much looking forward to these important results,” says Elin Trampe, CEO of Dicot Pharma.
About the phase 2a study
The purpose of the phase 2a study is to evaluate the effect of LIB-01 on erectile function in men with erectile dysfunction. Each subject participates in the study for eight weeks after dosing. The efficacy of LIB-01 is evaluated using the International Index of Erectile Function questionnaire. The trial is double blind and placebo controlled. This means that neither the clinical staff administering the study drug, nor the participants, know which subjects are receiving LIB-01 and which are receiving placebo.