deltatrials
Completed PHASE1 INTERVENTIONAL 2-arm NCT01113281

Dose-Escalation Study on Safety and Immunogenicity of VPM1002 in Comparison to BCG in Healthy Volunteers in South Africa

Phase Ib Open Label, Randomized, Controlled, Dose-Escalation Study to Evaluate Safety and Immunogenicity of VPM1002 in Comparison With BCG in Healthy Volunteers in South Africa

Sponsor: Farmovs-Parexel Bloemfontein, Republic of South Africa (Clinical Site)

Conditions Tuberculosis
Updated 6 times since 2017 Last updated: Nov 18, 2011 Started: Apr 30, 2010 Primary completion: Dec 31, 2010 Completion: Mar 31, 2011
This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

Listed as NCT01113281, this PHASE1 trial focuses on Tuberculosis and remains completed. Sponsored by Farmovs-Parexel Bloemfontein, Republic of South Africa (Clinical Site), it has been updated 6 times since 2010, reflecting limited change activity. This study is part of the global effort to build evidence for infectious disease interventions.

Status Flow

~Jan 2017 – ~Jun 2018 · 17 months · monthly snapshotCompleted~Jun 2018 – ~Jan 2021 · 31 months · monthly snapshotCompleted~Jan 2021 – ~Jul 2024 · 42 months · monthly snapshotCompleted~Jul 2024 – ~Sep 2024 · 2 months · monthly snapshotCompleted~Sep 2024 – ~Aug 2025 · 11 months · monthly snapshotCompleted~Aug 2025 – present · 11 months · monthly snapshotCompleted

Change History

6 versions recorded
  1. Aug 2025 — Present [monthly]

    Completed PHASE1

  2. Sep 2024 — Aug 2025 [monthly]

    Completed PHASE1

  3. Jul 2024 — Sep 2024 [monthly]

    Completed PHASE1

  4. Jan 2021 — Jul 2024 [monthly]

    Completed PHASE1

  5. Jun 2018 — Jan 2021 [monthly]

    Completed PHASE1

Show 1 earlier version
  1. Jan 2017 — Jun 2018 [monthly]

    Completed PHASE1

    First recorded

Apr 2010

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:
  • Farmovs-Parexel Bloemfontein, Republic of South Africa (Clinical Site)
  • HJ-CTC George, RSA (Statistics & Report)
  • Serum Life Science Europe GmbH
  • Triclinium Johannesburg, RSA (Monitoring and Overall Management of the study)
  • University of Stellenbosch
Data source: Serum Life Science Europe GmbH

For direct contact, visit the study record on ClinicalTrials.gov .

Study Locations