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A Phase 1-2 Study of PRT-201 Administered in Chronic Kidney Disease (CKD) Patients

P

Proteon Therapeutics

Status and phase

Completed
Phase 2
Phase 1

Conditions

Chronic Kidney Disease

Treatments

Drug: PRT-201

Study type

Interventional

Funder types

Industry

Identifiers

NCT00679991
PRT-201-101

Details and patient eligibility

About

PRT-201 is a protein that causes long lasting dilation of blood vessels when applied to the outside surface of the blood vessel. The purpose of this study is to determine if PRT-201, when applied to a limited segment of blood vessel immediately after surgery to create an arteriovenous fistula (AVF), is safe, dilates the blood vessel, and increases blood flow through the AVF.

Enrollment

66 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age of at least 18 years.
  • Chronic kidney disease with anticipated start of hemodialysis within six months or current hemodialysis dependence.
  • Planned creation of a new AVF.

Exclusion criteria

  • Patients for whom this is the only potential site for an AVF.
  • By physical examination, absence of radial or ulnar artery flow or non-patent palmer arch.
  • Treatment with any investigational agent within the previous 30 days or investigational antibody therapy within 90 days of signing informed consent.
  • Pregnancy, lactation or plans to become pregnant during the course of the study.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

66 participants in 2 patient groups, including a placebo group

PRT-201
Active Comparator group
Treatment:
Drug: PRT-201
Drug: PRT-201
2
Placebo Comparator group
Treatment:
Drug: PRT-201
Drug: PRT-201

Trial contacts and locations

11

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Data sourced from clinicaltrials.gov

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