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MT1002 for Injection for Acute Coronary Syndrome

Phase 1
Waitlist Available
Research Sponsored by Shaanxi Micot Technology Limited Company
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 30 days
Awards & highlights

Study Summary

This trial is studying how safe and effective a new drug is in people with and without a certain medical condition.

Eligible Conditions
  • Acute Coronary Syndrome

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~30 days
This trial's timeline: 3 weeks for screening, Varies for treatment, and 30 days for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Plasma PK
Urine PK
plasma PK
Secondary outcome measures
Adverse events

Trial Design

2Treatment groups
Experimental Treatment
Group I: Renal impairmentExperimental Treatment1 Intervention
moderate and severe Renal impairment subjects
Group II: Healthy controlExperimental Treatment1 Intervention
Healthy control subjects with normal renal function

Find a Location

Logistics

Participation is compensated

You will be compensated for participating in this trial.

Who is running the clinical trial?

Shaanxi Micot Technology Limited CompanyLead Sponsor
4 Previous Clinical Trials
136 Total Patients Enrolled
1 Trials studying Acute Coronary Syndrome
6 Patients Enrolled for Acute Coronary Syndrome

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Do I fulfill the qualifications needed to participate in this research?

"This clinical trial is in search of 24 people diagnosed with acute coronary syndrome, aged between 18 and 80. Exclusion criteria include: post-menopausal or surgically sterile patients; males who have not had a vasectomy for at least three months prior to dosing and are sexually active with fertile partners must agree to use reliable contraception methods from commencement of treatment until 90 days after the study's end; those without any serious neurological, cardiovascular, respiratory, immunological etc illnesses within four weeks before drug administration; non-smokers with BMI greater than 18.0 and lesser than 40.0 kg/m2 as well as body weight above"

Answered by AI

Are geriatric individuals being included in the recruitment process for this trial?

"This research initiative is searching for individuals between 18 and 80 years of age."

Answered by AI

Are there any more openings for participants to join this trial?

"According to the information provided on clinicaltrials.gov, this research study is recruiting participants now. The trial was initially posted on April 15th 2022 and revised most recently on October 24th 2022."

Answered by AI

How many participants is this clinical trial accepting?

"Affirmative, the information on clinicaltrials.gov confirms that this experiment is presently enrolling patients. It was first made available on April 15th 2022, and last edited two months ago in October 24th 2022. The trial requires a total of 24 study participants to be recruited at one site."

Answered by AI

To what degree does MT1002 for Injection pose a risk to patients?

"Our team at Power assigned MT1002 for Injection a rating of 1, as the current evidence suggests it has limited efficacy and safety data from Phase 1 trials."

Answered by AI
~1 spots leftby Apr 2025