Overview

Phase I Drug Trial for S/E of Marimastat in Disabling Malformations When no Other Options.

Status:
Completed
Trial end date:
2007-10-01
Target enrollment:
0
Participant gender:
All
Summary
3 patients were enrolled in each of 3 study cohorts. There three cohorts were given differing, incrementally larger doses of this phase I drug. The same safety measures are being obtained on all patients. Efficacy measures were individualized as enrolllees do not have the same underlying vascular anomaly. The study is structured to include a 24 month drug-phase and a 24 month follow-up phase. The study is now closed to enrollment.
Phase:
Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Boston Children's Hospital
Boston Children’s Hospital
Treatments:
Marimastat
Criteria
Inclusion Criteria:

- Patient with vascular malformation causing risk of one or more of the following based
on unanimous assessment of designated physicians in the multidisciplinary Vascular
Anomalies Team.

- airway/respiratory/visual/auditory/neurologic compromise;

- high output cardiac failure;

- life-threatening or disabling hemorrhage(cutaneous/GI/intracranial/
parenchymal/cavitary);

- skeletal distortion/destruction/erosion;

- life-threatening or disabling soft tissue distortion or destruction

- Patient must be felt to have failed, be unable to significantly benefit from, or be at
risk for other available therapies, including surgeries, embolization, and
sclerotherapy based on unanimous assessment of designated physicians in the
multidisciplinary Vascular Anomalies Team.

- Patient must be felt to have one or more physical, imaging, photographic, physiologic
or other measurable features that can be measured on a regular basis for preliminary
evaluation of efficacy. The feature(s) must be agreed on by the designated physicians
in the multidisciplinary Vascular Anomalies Team).

- Signed Patient informed consent.

Exclusion Criteria:

- Pregnancy

- Patient nursing child.

- Female patient of childbearing potential unwilling to receive contraceptive counseling
and use reliable contraceptive method.

- Patient enrolled in any other clinical trial involving an investigational agent
(unless approved by the designated physicians on the multidisciplinary team)

- Parent or guardian or child unwilling to provide consent or assent.