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Virus Therapy

Zofin Plus Standard Care for COVID-19

Phase 1 & 2
Waitlist Available
Led By Odalys P Frontela, MD
Research Sponsored by ZEO ScientifiX, Inc.
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 day 0, day 4, day 8, day14, day 21, day 28
Awards & highlights

Study Summary

This trial will test if Zofin is safe and effective for treating moderate to severe SARS related to COVID-19 infection.

Eligible Conditions
  • COVID-19
  • Coronavirus
  • Acute Respiratory Distress Syndrome

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~day 0, day 4, day 8, day14, day 21, day 28
This trial's timeline: 3 weeks for screening, Varies for treatment, and day 0, day 4, day 8, day14, day 21, day 28 for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Incidence of Severe Adverse Events
Incidence of any infusion associated adverse events
Secondary outcome measures
All Cause Mortality
C-reactive protein Levels
Chest Imaging Changes
+5 more

Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: Zofin Plus Standard CareExperimental Treatment1 Intervention
Participants in this group will receive standard of care plus Zofin on day 0, day 4 and day 8.
Group II: Placebo Plus Standard CarePlacebo Group1 Intervention
Participants in this group will receive standard of care plus placebo (Saline) on day 0, day 4 and day 8.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Zofin
2022
Completed Phase 2
~40

Find a Location

Who is running the clinical trial?

ZEO ScientifiX, Inc.Lead Sponsor
3 Previous Clinical Trials
38 Total Patients Enrolled
2 Trials studying COVID-19
18 Patients Enrolled for COVID-19
Organicell Regenerative MedicineLead Sponsor
3 Previous Clinical Trials
38 Total Patients Enrolled
2 Trials studying COVID-19
18 Patients Enrolled for COVID-19
Odalys P Frontela, MDPrincipal InvestigatorCo-Investigator

Frequently Asked Questions

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

Is this investigation pioneering a new approach?

"Research into Zofin Plus Standard Care commenced in 2020, led by Organicell Regenerative Medicine. Subsequent to the initial investigation involving 20 patients, it successfully passed through its Phase 1 & 2 clinical trial stages. At present there is one live study being sponsored by Organicell Regenerative Medicine exploring this therapeutic option."

Answered by AI

What is the scope of participation for this clinical trial?

"Unfortunately, this clinical test is not presently accepting applicants. It was initially posted on September 8th 2020 and last modified nearly two years later on the 19th of September 2022. For those seeking other trials, 1887 studies connected to Covid-19 are currently enrolling participants while one research project related to Zofin Plus Standard Care remains open for enrolment."

Answered by AI

Is there still capacity for participants in this trial?

"At this point in time, the trial is not enrolling participants. The research initiative was first introduced on September 8th 2020 and edited lastly on September 19th 2022. If you are searching for alternative studies, 1887 clinical trials concerning COVID-19 (pathology) and 1 study about Zofin Plus Standard Care are actively recruiting patients."

Answered by AI

Are there any other independent studies done using Zofin Plus Standard Care?

"Currently, there is one ongoing clinical trial studying the efficacy of Zofin Plus Standard Care. This research project has not progressed to Phase 3 yet, though it is taking place in three different locations within New york City."

Answered by AI

What results are researchers hoping to obtain from this clinical trial?

"According to the report by Organicell Regenerative Medicine, their primary objective is to measure Incidence of Severe Adverse Events over a two-month period. Secondary outcome metrics include All Cause Mortality (as assessed at day 60 or hospital discharge), Quantification of COVID-19 (through viral load analysis and nose/throat swabs) as well as Chest Imaging Changes (including Ground Glass Opacity, Local Patchy Shadowing, Bilateral Patchy Shadowing and Interstitial Abnormalities)."

Answered by AI
~4 spots leftby Apr 2025