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Long-Term Follow-up Study of Patients Who Received PB127 Ultrasound Imaging Agent

P

POINT Biopharma

Status

Terminated

Conditions

Coronary Artery Disease

Study type

Observational

Funder types

Industry

Identifiers

NCT00584714
127-014-A

Details and patient eligibility

About

The purpose of this study is to collect longer term follow-up information concerning health and survival on selected patients who received PB127 for injectable suspension in the pivotal trial (127-014).

Enrollment

300 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

Patients enrolled in Protocol 127-014 who

  1. Were enrolled in Stratum 1
  2. Did not undergo angiography during study evaluation
  3. Did not have a clinical oucome during the initial 6 month follow-up period as described in Protocol 127-014.

Trial contacts and locations

39

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Data sourced from clinicaltrials.gov

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