TheraRadar
Data updated: May 26, 2026

regenecyte (hpc, cord blood)

Approved 2024-11-20
1
Indication
--
Phase 3 Trials
1
Years on Market

Details

Status
Prescription
First Approved
2024-11-20
Routes
Intravenous
Dosage Forms
Injection

Companies

Active Ingredient: HPC, Cord Blood

regenecyte Approval History

2025
2026
Original
New Indication
New Form
Label Update
1 FDA actions from 2024 to 2024
Nov 2024 ORIGINAL
Update · CBER biologic (Purple Book)

What regenecyte Treats

1 FDA approvals

Originally approved for its first indication in 2024 .

  • Other (1)
📋

Clinical Trial Registry

2 trials
Trial Sponsor ID Phase Status Title
NCT07184385 SCUS002 Ph 3 not yet recruiting A Study of Human Umbilical Cord Blood (REGENECYTE) Infusion in Patients With Post-COVID Condition
NCT05682560 SCUS001 Ph 2 completed Human Umbilical Cord Blood (RegeneCyte) Infusion in Patients with Post-COVID Syndrome
🔬

Active Pipeline

Pro

Ongoing clinical trials by development phase

Loading...

Key Completed Trials

Pro

Completed studies with published results, ranked by significance

Loading...
📊

Trial Timeline

Full development history with FDA approval milestones

|
Loading...
Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

regenecyte FDA Label Details

Track regenecyte with TheraRadar Pro

Watchlist alerts, full database access, CSV exports across 14,000+ drugs.

Upgrade to Pro

Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.