20+years of experienceCheck current recruitment and learn how participation in a clinical trial works.
Clinical trial for people with depression and sleep-related symptoms.
Learn moreRecruitment openStudy of an investigational psychedelic with structured psychological support in depression.
Learn moreActive — not recruitingClinical research with COMP360 psilocybin for people with treatment-resistant depression.
Learn moreActive — not recruitingStudy for people with mild cognitive impairment or early-stage Alzheimer's disease.
Learn moreEach clinical trial has specific inclusion and exclusion criteria. Participation is possible after medical assessment, protocol review and informed consent.
Participants do not pay for procedures required by the study protocol. Travel reimbursement, additional support and arrangements for medical events depend on the specific protocol and the documents provided before informed consent.
People interested in participation can contact the site reception or the clinical research coordinator.
Participants do not pay for procedures required by the study protocol. Travel reimbursement, additional support and arrangements for medical events depend on the specific protocol and informed-consent documents; the coordinator explains them before screening.
Yes. Participants may withdraw according to the informed consent process without losing their right to regular medical care.
Placebo is an inactive comparator used in some studies. The protocol explains whether placebo may be used and how randomization works.