An Open Label Continuation Study of TRC105 Therapy for Patients Who Have Completed a Prior TRC105 Trial and Are Judged by the Investigator to Have the Potential to Benefit From Continued TRC105 Therapy

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Status: Enrolling by Invitation


This is a multicenter, open-label, non-randomized, study of TRC105 in patients that have completed a previous TRC105 study and are judged by the investigator to have the potential to benefit from continued TRC105 therapy.

Eligibility Criteria

Inclusion Criteria

  • Participation in a TRACON Pharmaceuticals sponsored parent TRC105 study and, thought to have potential to derive clinical benefit from continued treatment with TRC105 in the opinion of the parent study investigator.
  • Willing and able to consent for self to participate in study
  • Willing and able to comply with scheduled visits, treatment plan, laboratory tests, and other study procedures.
  • 18 years of age or older
  • ability to begin TRC105 dosing on this protocol within 6 weeks from the subjects last dose of TRC105 in the parent TRC105 study

Exclusion Criteria

  • Any clinical event that would make TRC105 therapy inappropriate under the parent protocol
  • Current treatment in another clinical study
  • Pregnant or breastfeeding
  • Other severe acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or study drug administration, or may interfere with the interpretation of study results, and in the judgment of the investigator, would make the subject inappropriate for entry into the study

Locations & Contacts

See trial information on for a list of participating sites.

Trial Phase & Type

Trial Phase

Phase I/II

Trial Type


Lead Organization

Lead Organization
TRACON Pharmaceuticals

Trial IDs

Primary ID 105CON101
Secondary IDs NCI-2013-00735 ID NCT02354612