Study of Safety and Tolerability of UNIFUZOL (Solution for Infusions) in Healthy Volunteers
Open Randomized Study of the Safety, Tolerability, and Pharmacokinetic Parameters of UNIFUZOL® (Solution for Infusions, 1.4%, Manufactured by NTFFPOLYSAN Ltd.,Russia) in Healthy Volunteers at Different Rates of Administration (Phase I)
Sponsor: POLYSAN Scientific & Technological Pharmaceutical Company
A PHASE1 clinical study on Peripheral Vascular Disease, this trial is completed. The trial is conducted by POLYSAN Scientific & Technological Pharmaceutical Company and has accumulated 9 data snapshots since 2016. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.
Status Flow
Change History
9 versions recorded-
Sep 2025 — Present [monthly]
Completed PHASE1
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Sep 2024 — Sep 2025 [monthly]
Completed PHASE1
-
Jul 2024 — Sep 2024 [monthly]
Completed PHASE1
-
Jan 2021 — Jul 2024 [monthly]
Completed PHASE1
-
Aug 2020 — Jan 2021 [monthly]
Completed PHASE1
▶ Show 4 earlier versions
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Mar 2019 — Aug 2020 [monthly]
Completed PHASE1
-
Jun 2018 — Mar 2019 [monthly]
Completed PHASE1
-
Feb 2018 — Jun 2018 [monthly]
Completed PHASE1
Status: Recruiting → Completed
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Feb 2017 — Feb 2018 [monthly]
Recruiting PHASE1
First recorded
Jul 2016
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- POLYSAN Scientific & Technological Pharmaceutical Company
For direct contact, visit the study record on ClinicalTrials.gov .