Purpose of this Study
We are doing this study to find the most effective, safe dose of an experimental drug called DISC-3405 (the study drug) in adults with polycythemia vera (PV).
Who Can Participate?
Eligibility
Adults ages 18+ who:
- Are diagnosed with PV
- Do not have any clinically significant for of thrombosis (e.g., deep vein thrombosis or splenic vein thrombosis) for at least 2 months before beginning the study regimen
- Have no history of invasive malignancies within the last 5 years, except localized, cured prostate cancer and cervical cancer, or other malignancies deemed acceptable by the sponsor
- Have not received busulfan, pipobroman, or phosphorus-32 for at least 7 months before joining the study
Age Range
18-110
Sex/Genders
Male (cisgender)
Female (cisgender)
Non-binary or gender fluid
Transgender male
Transgender female
Looking for Healthy Participants
No
What is Involved?
Description
If you choose to join this study, participation will consist of 5 periods: the screening period, the observation period, the study drug period, the optional continuation period, and the follow-up period.
Screening Period: This period will last about 7 days and involve a visit to our clinic for a physical exam and blood draws to confirm your eligibility to take part in the study.
Observation Period: This period will involve up to 4 visits, and it will be used to establish a prospective baseline of your typical routine care. During this time period (4 to 12 weeks before your first dose of study drug), you will be treated with your normal standard of care and have some extra blood tests and questionnaires. You will not get the study drug during this period.
Study Drug Period: You will get the study drug during this period. It will last about a year and involve up to 26 visits to our clinic.
Continuation Period: This period is optional. During this period, you can continue to take the study drug for up to 2 more years. You will continue to come in for visits similar to during the study drug period, but the visits will be less frequent.
Follow-up Period: This period will last for 4 weeks after you stop taking the study drug.
Locations
Duke University Hospital
Visit Timing
Weekdays
Compensation
No
Spanish Materials Available
No
Study Details
Full Title
A Phase 2a, Open-Label Study of the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Efficacy of DISC-3405 in Participants with Polycythemia Vera (PV)
Principal Investigator
Lindsay
Rein
Protocol Number
PRO00118054
NCT ID
NCT06985147
Phase
II
Enrollment Status
Pending Open to Enrollment