A Study to Evaluate Long-term Safety in Subjects Who Have Participated in Other Luspatercept (ACE-536) Clinical Trials
Status:
Recruiting
Trial end date:
2030-03-25
Target enrollment:
Participant gender:
Summary
A Phase 3b, open-label, single-arm, rollover study to evaluate the long-term safety of
luspatercept, to the following subjects:
- Subjects receiving luspatercept on a parent protocol at the time of their transition to
the rollover study, who tolerate the protocol-prescribed regimen in the parent trial
and, in the opinion of the investigator, may derive clinical benefit in the opinion of
the investigator from continuing treatment with luspatercept.
- Placebo arm subjects from parent protocol (at the time of unblinding or in follow-up)
crossing over to luspatercept treatment (provided subjects have met all requirements for
entering the rollover study as per the parent protocol).
- Subjects in the follow-up phase previously treated with luspatercept or placebo in the
parent protocol will continue into long-term post-treatment follow-up in the rollover
study until the follow-up commitments are met (unless they meet requirements as per
parent protocol to cross-over to luspatercept treatment).
The study design is divided into the Transition Phase, Treatment Phase and Follow-up Phase.
Subjects will enter transition phase and depending on their background will enter either the
treatment phase or the Long-term Post-treatment Follow-up (LTPTFU) phase.
- Transition Phase (Screening): up to 21 days prior to enrollment
- Treatment Phase: For subjects in luspatercept treatment the dose and schedule of
luspatercept in this study will be the same as the last dose and schedule in the parent
luspatercept study. For placebo arm subjects from parent protocol (at the time of
unblinding or in follow-up) crossing over to luspatercept treatment (provided subjects
have met all requirements for entering the rollover study as per the parent protocol)
will start at a luspatercept dose of 1.0 mg/kg every 3 weeks (Q3W). This does not apply
to subjects that are in long-term follow-up from the parent protocol.
- Follow-up Phase:
- 42 Day Safety Follow-up Phase: subjects will be followed for 42 days after the last
dose of luspatercept, for the assessment of safety-related parameters and adverse
event (AE) reporting.
- Long-term Post-treatment Follow-up (LTPTFU) Phase:
All subjects who are continuing in the LTPTFU Phase, will continue to be followed for 5 years
from Dose 1 of the parent protocol, or 3 years of post-treatment from last dose of the parent
protocol, whichever occurs later. Subjects will be followed every 6 months until death,
withdrawal of consent, study termination, or until a subject is lost to follow-up. Subjects
will also be monitored for progression to AML or any malignancies/pre- malignancies. New
anticancer or disease related therapies should be collected at the same time schedule.
Subjects transitioning from a parent luspatercept study in post-treatment follow-up (safety
or LTPTFU) will continue from the same equivalent point in this rollover study.
The rollover study will be terminated, and relevant subjects will discontinue from the study
when all subjects fulfill 5 years from Dose 1 of the parent protocol, or 3 years of
post-treatment from last dose of the parent protocol, whichever occurs later. The shift to
commercial drug is an alternative way to stop the study.