468 Participants Needed

CYB003 for Depression

(EXTEND Trial)

Recruiting at 9 trial locations
AG
SW
AM
CW
CD
Overseen ByClinical Development
Age: 18+
Sex: Any
Trial Phase: Phase 3
Sponsor: Cybin IRL Limited
Must be taking: Antidepressants
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Pivotal Trial (Near Approval)This treatment is in the last trial phase before FDA approval
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial focuses on assessing the long-term safety and effectiveness of CYB003 for treating major depressive disorder (MDD). Participants from previous CYB003 studies who either did not initially respond or responded but later relapsed will receive additional doses of CYB003. This trial suits those who completed earlier CYB003 trials and maintained the same dose of their antidepressant medication. As a Phase 3 trial, it represents the final step before FDA approval, providing participants an opportunity to contribute to the potential availability of a new MDD treatment.

Do I need to stop my current medications for the trial?

No, you do not need to stop your current medications. Participants must continue the same antidepressant medication at a stable dose throughout the trial.

Is there any evidence suggesting that CYB003 is likely to be safe for humans?

In a previous study, all participants responded positively to treatment with CYB003, and 71% were in remission 12 months after receiving just two 16 mg doses. This outcome suggests the treatment is well-tolerated. Research has also shown strong and lasting improvements in depression symptoms. The studies tested both the effectiveness and safety of CYB003, yielding positive results.

While specific side effects are not listed, ongoing trials suggest CYB003 is generally safe, with no major safety concerns reported so far. Participants in current trials will continue their usual antidepressants and receive psychological support, which aids in safety monitoring.12345

Why do researchers think this study treatment might be promising for depression?

Unlike the standard treatments for depression, which often include SSRIs or SNRIs, CYB003 is unique because it is a synthetic form of psilocybin, a compound found in psychedelic mushrooms. Researchers are excited about CYB003 because it targets the serotonin receptors in the brain in a novel way, potentially leading to rapid and profound changes in mood. While traditional antidepressants can take weeks to show effects, CYB003 may offer quicker relief for those who don't respond to conventional treatments, or who relapse after initially responding. This potential for faster action and effectiveness in difficult cases makes CYB003 a promising candidate in the fight against depression.

What evidence suggests that CYB003 might be an effective treatment for depression?

Research has shown that CYB003 is promising for treating major depressive disorder (MDD). In earlier studies, all participants responded well to the treatment, and 71% were free of depression symptoms a year after receiving just two doses of 16 mg each. The treatment demonstrated strong and lasting improvements in symptoms over four months. CYB003, which participants in this trial will receive, is a modified version of a compound found in psychedelic mushrooms, known for its mood-enhancing effects. These findings suggest CYB003 could effectively reduce symptoms of depression.12356

Who Is on the Research Team?

CD

Clinical Development

Principal Investigator

Cybin IRL Limited

Are You a Good Fit for This Trial?

This trial is for individuals who have completed previous CYB003 trials for Major Depressive Disorder (MDD) and remained on a stable antidepressant dose. They must consent to the study's requirements, not be pregnant, and use effective contraception if they can have children.

Inclusion Criteria

I will use a condom and spermicide, and my partner will use effective birth control during and after the trial.
I will use effective birth control and a condom during the trial and for 12 weeks after.
I completed the CYB003-002 APPROACH or CYB003-003 EMBRACE trial and received both doses.
See 3 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive 16 mg of CYB003 in 2 medicine sessions, approximately three weeks apart, with an optional additional dose if relapse occurs

12 weeks
Multiple visits as per dosing schedule

Follow-up

Participants are monitored for safety and effectiveness after treatment

16 weeks
Regular assessments at specified days

Open-label extension

Participants may continue receiving CYB003 to assess long-term safety and efficacy

Long-term

What Are the Treatments Tested in This Trial?

Interventions

  • CYB003
Trial Overview The EXTEND trial is testing the long-term safety and effectiveness of a drug called CYB003 in treating MDD. It follows up on earlier double-blind studies to monitor ongoing effects in participants.
How Is the Trial Designed?
1Treatment groups
Experimental Treatment
Group I: CYB003Experimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Cybin IRL Limited

Lead Sponsor

Trials
5
Recruited
860+

Worldwide Clinical Trials

Collaborator

Trials
70
Recruited
15,800+

Citations

Cybin Reports Positive Phase 2 Data for CYB003 ...100% of participants were responsive to treatment and 71% of participants were in remission at 12 months after just two 16 mg doses of CYB003.
"A Study of a Deuterated Psilocin Analog (CYB003) in ...The purpose of this study is to examine the efficacy, safety, and tolerability of CYB003 compared to matching placebo as adjunctive treatment in ...
CYB003 for the Adjunctive Treatment of Major Depressive ...CYB003 already saw positive 4-month efficacy data in MDD in phase 2 studies. Investigators noted robust and sustained improvements in symptoms ...
Efficacy and safety of psilocybin in the treatment of Major ...This meta-analysis supports psilocybin's efficacy in treating MDD, particularly at a 25 mg dose, showing a time-dependent therapeutic effect.
A Study of a Psilocybin Analog (CYB003) in Healthy ...The purpose of this study is to determine the safety and tolerability of ascending oral doses of CYB003 in healthy participants with and without major ...
FDA Breakthrough Therapy Designation Granted to Novel ...Efficacy and Safety Data: Data from the phase 2 trial of CYB003 for MDD showed robust and sustained improvements in depression symptoms, with ...
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