Principal Investigator
Enrollment Status
Clinical Trial ID
Clinical Trial Summary
This is an open-label study to evaluate the long-term efficacy and safety of KZR-616 in
patients with active PM or DM who completed the double-blind treatment period of Study
KZR-616-003, up to and including the Week 32 Visit, prior to the first dose of open-label
KZR-616.
Phase
Phase 2
Funding Agency/Sponsor
Industry
Disease
Neuro-Muscular Disorders
Enrollment Eligibility
Inclusion Criteria:
- Must have successfully completed Study KZR-616-003 through Week 32, including the Week
32 Visit assessments
- Women of childbearing potential (WOCBP) must have a negative urine or serum pregnancy
test prior to the first dose of KZR-616 in KZR-616-003E, and must agree to continue to
use a highly effective method of birth control until completion of the study.
- Male patients must continue to use an effective contraception method for 1 week
following their last dose of KZR-616 or be congenitally or surgically sterile.
Exclusion Criteria:
- Have clinical evidence of significant unstable or uncontrolled diseases other than the
disease under study, that in the opinion of the Investigator or Sponsor/designee,
could confound the results of the study, put the patient at undue risk, or interfere
with protocol adherence.
- Has participated in any clinical study other than KZR-616-003 between the Week 32
Visit of Study KZR-616-003 and the first study visit of KZR-616-003E, if they are not
on the same calendar day.
- Are females who are breastfeeding or who plan to become pregnant during the study, or
who are actively trying to conceive at the time of signing of the informed consent
form.
- Have hypersensitivity to KZR-616 or any of its excipients.