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Long-term Follow-up Study Following the Approval of Hearticellgram-AMI Administration

Long-term Follow-up Study Following the Approval of Hearticellgram-AMI Administration to Evaluate Its Safety in Patients With Acute Myocardial Infarction

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07400458
Enrollment
100
Registered
2026-02-10
Start date
2022-03-03
Completion date
2032-09-30
Last updated
2026-02-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Myocardial Infarction

Brief summary

This Long-term follow-up is designed to evaluate the safety of patient with Acute Myocardial Infarction who had administered Hearticellgram-AMI.

Detailed description

To evaluate the safety for 60 months after a single dose of Hearticellgram-AMI in patients with Acute Myocardial Infarction.

Interventions

Patients who had administered Hearticellgram-AMI.

Sponsors

Pharmicell Co., Ltd.
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

1. Those who had administered Hearticellgram-AMI 2. Those who voluntarily agreed in writing to participate in this investigation

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frameDescription
Rate of AESIFor 5 yearsdeath, neoplasms or malignancies in tissues or organs, Immune response

Countries

South Korea

Contacts

CONTACTDAEUN JUNG
daeun4100@pharmicell.com82-2-3496-0134

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026