Treatment-resistant depression
Treatment-resistant depression · Alzheimer's disease
Clinical trials · Bydgoszcz, Poland
Treatment-resistant depression, Alzheimer's disease - clinical trials
Promente conducts controlled clinical trials of investigational substances and procedures in defined indications: depression, treatment-resistant depression (TRD), Alzheimer's disease, mild cognitive impairment and other neurodegenerative disorders. Participation always depends on protocol criteria, medical eligibility assessment and informed consent.
How we work
Clinical trials require precision, not promises.
Clinical experience
Projects run by experienced physicians, in collaboration with a highly qualified nursing and psychological team.
Safety
Eligibility assessment, informed consent, monitoring and the right to withdraw at every stage.
Transparency
Educational content does not replace medical consultation or eligibility assessment for a study protocol.
Current recruitment
See which studies we support and how you can participate
Recruitment open
KOASTAL-3
Clinical trial of an investigational molecule intended for patients with depression.
Learn moreRecruitment openOARS7
Clinical trial of an investigational molecule intended for patients with depression.
Learn moreRecruitment openEMBRACE CYB003-003
Clinical trial of an investigational molecule intended for patients with depression.
Learn moreStudies we are currently conducting
Active research projects under the care of the Promente team
In progress
COMP 006
Clinical research with COMP360 psilocybin for patients with treatment-resistant depression (TRD).
Learn moreIn progress
BIOGEN "Celia"
The study is intended for people with mild cognitive impairment and early-stage Alzheimer's disease.
Complete the formDear Patients
Please note that medical services in psychogeriatric, neurological and neuropsychological outpatient care are currently provided by Centrum Medyczne Propsyche. Our centers are located at the same address.
Promente currently focuses exclusively on conducting clinical trials.
You are warmly invited to use our services.
The Propsyche and Promente Team
Outpatient center websiteWhat should you know about clinical trials?
Clinical trials are a key stage in evaluating investigational medicines and procedures before they may be considered for wider use.
Clinical trials are designed to assess the safety and activity of an investigational method under controlled conditions. Their course is closely supervised not only by medical specialists, but also by independent bioethics committees that protect participants and ensure that studies comply with ethical standards.
Clinical trials involve patients and healthy volunteers, and all procedures are carefully planned and approved by the relevant authorities. Study results help develop medical knowledge and inform decisions about further evaluation or use of investigational methods.
Clinical trial phases
Clinical trials consist of several stages
Phase I
Safety testing in small groups of volunteers
Phase II
Assessment of safety, activity and appropriate dosing
Phase III
Comparative studies conducted in larger patient groups
Phase IV
Monitoring after a medicine has entered the market
"Clinical trials are a key element of medical development. They allow investigational methods to be assessed under controlled conditions, without promising an effect for any individual participant."
Learn more about clinical trials
See current clinical trials or learn about collaboration opportunities with our center