Ultramicronized Palmitoylethanolamide (PEA) Treatment in Hospitalized Participants With COVID-19

• Sponsor: FSD Pharma, Inc. (Industry)
• Overall Status: Terminated
• CT.gov ID: NCT04619706
• Collaborator: (none)
• Enrollment: 53
• Locations: 10
• Arms: 3
• Actual Duration (Months): 8.3
• Patients Per Site: 5.3
• Patients Per Site Per Month: 0.6

Study Details

Study Description

Brief Summary

This study will measure the effect of FSD201 (ultramicronized PEA) + SoC vs placebo + SoC on Day 28, on disease progression in the confirmed coronavirus disease 2019 (COVID-19) patient population.

Condition or Disease	Intervention/Treatment	Phase
COVID-19	Drug: FSD201; Drug: Placebo	Phase 2

Study Design

• Study Type: Interventional
• Actual Enrollment: 53 participants
• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
• Primary Purpose: Treatment
• Official Title: A Randomized, Double-Blind, Placebo-Controlled, Multicenter Phase IIA Study of FSD201 (Ultramicronized PEA) + Standard of Care (SOC) Vs SOC in the Treatment of Hospitalized Patients With COVID-19
• Actual Study Start Date: Dec 14, 2020
• Actual Primary Completion Date: Aug 24, 2021
• Actual Study Completion Date: Aug 24, 2021

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Arm A: FSD201 600 mg Participants will receive 600 milligrams (mg) FSD201 tablet twice daily (BID) orally along with the placebo matched to 600 mg FSD201 tablet from Day 1 to Day 14.	Drug: FSD201; Tablets for oral administration.; Other Names: ultramicronized palmitoylethanolamide (PEA) ; Drug: Placebo; Placebo tablets matched to FSD201 for oral administration.
Experimental: Arm B: FSD201 1200 mg Participants will receive 1200 mg (2x600 mg) tablets FSD201 BID orally from Day 1 to Day 14.	Drug: FSD201; Tablets for oral administration.; Other Names: ultramicronized palmitoylethanolamide (PEA)
Placebo Comparator: Arm C: Placebo Participants will receive placebo matched to 600 mg FSD201 tablets (2xplacebo tablets) from Day 1 to Day 14.	Drug: Placebo; Placebo tablets matched to FSD201 for oral administration.

Outcome Measures

Primary Outcome Measures

1. Percentage of Participants With Disease Progression at Day 28 [Day 28]

   Disease progression will be defined as the percentage of participants who are not alive or who have respiratory failure. Respiratory failure will be defined as the need for invasive or non-invasive mechanical ventilation, high-flow oxygen, or extracorporeal membraneoxygenation (ECMO).

Secondary Outcome Measures

1. Percentage of Participants With Disease Resolution at Day 28 [Day 28]

   Disease resolution will be defined as participants alive and not requiring supplemental oxygen (at home or in the hospital).

2. Percentage of Participants Requiring Invasive Mechanical Ventilation or ExtraCorporeal Membrane Oxygenation (ECMO) or who are not Alive on Day 28 [Day 28]

3. Change From Baseline in Oxygen use [Baseline, Day 15, and Day 28]

   Oxygen use will be assessed by change in the type of oxygen use between the following categories: no oxygen, supplemental oxygen, non-invasive mechanical ventilation or high-flow oxygen, invasive mechanical ventilation/ECMO.

4. Change From Baseline in Saturation of Oxygen (SpO2) percent (%) [Baseline through Day 28]

5. Change From Baseline in Clinical Status Related to COVID-19 [Baseline, Day 15, and Day 28]

   Clinical status will be measured with the 9-point ordinal scale ranging (1-9; 1 being death and 9 being not hospitalized, not requiring supplemental home oxygen, and no limitations on activities).

6. Percentage of Participants who Die (Mortality Rate) at Day 28 [Day 28]

   Mortality rate will be defined as the percentage of participants who die.

7. Percentage of Participants Testing Negative for COVID-19 at Day 28 [Day 28]

   COVID-19 testing by standard standard reverse transcription-polymerase chain reaction (RT-PCR) assay or equivalent test.

8. Number of Participants with Adverse Events (AEs) and Serious Adverse Events (SAEs) [From the signing of the informed consent to Day 60 (approximately 9 months)]

   Number of participants with AEs and SAEs will be summarized and reported by seriousness, severity, relationship to the study medication, outcome, and duration.

9. Number of Participants With Clinically Significant Changes in Vital Signs, Laboratory Parameters, Electrocardiogram Findings and Physical Examination Findings [Baseline through Day 28]

   The number of participants with clinically significant changes in vital signs, laboratory parameters and electrocardiogram findings, and physical findings will be reported.

10. Plasma Concentrations of FSD201 [Day 1 and Day 14]

    Plasma concentrations will be measured in participants who give optional consent will be collected relative to the first dose on Day 1 and the first dose on Day 14. Samples on Day 1 and Day 14 will be collected predose (within 10 minutes before the first daily dose) and post dose at 2 hours (±30 minutes), 12 hours (±30 minutes) (before the evening dose), and 24 hours (±30 minutes)(before the next morning dose).

11. Maximum Observed Plasma Concentration (Cmax) of FSD201 [Day 1 and Day 14]

    Cmax is defined as maximum observed plasma concentration.

12. Area Under the Concentration-Time Curve (AUC) of FSD201 [Day 1 and Day 14]

    Area under the concentration-time curve (AUC).

13. Elimination Half-Life (t1/2) [Day 1 and Day 14]

    Elimination half-life (t1/2) of FSD201.

14. Apparent Total Body Clearance (CL/F) of FSD201 [Day 1 and Day 14]

    CL/F is the apparent total body clearance of FSD201 in plasma.

15. Apparent Volume of Distribution (Vz/F) of FSD201 [Day 1 and Day 14]

    Vz/F is the apparent volume of distribution of FSD201 in plasma.

16. Average Observed Plasma Concentration at Steady State (Cav) of FSD201 [Day 1 and Day 14]

    Cav is average plasma concentration over a dosing interval.

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years and Older
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Inclusion Criteria:

• Must be willing and able to give informed consent to participate in the study

• Has admitted to a hospital and has a positive severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) test by standard reverse transcription-polymerase chain reaction (RT-PCR) assay or equivalent test

• Has the presence of any symptom(s) suggestive of moderate or severe systemic illness with COVID-19 on Day 1 such as the presence of fever (greater than or equal to (>=)38.0 degree Celsius [>=100.4 degree fahrenheit] by any route), "feeling hot," "feeling sweaty," headache, malaise, fatigue, muscle pain, diarrhea, nausea, vomiting, cough, sore throat, or shortness of breath upon exertion and/or at rest, or respiratory distress

• Has the presence of moderate to severe clinical signs indicative of moderate or severe illness with COVID-19 on Day 1. A. Moderate: (1) Clinical signs suggestive of moderate illness with COVID-19, such as respiratory rate >=20 breaths per minute, SpO2 >93% on room air at sea level, heart rate >=90 beats per minute. (2) No clinical signs indicative of severe or critical COVID-19. B. Severe: (1) Clinical signs suggestive of severe systemic illness with COVID-19, such as respiratory rate >=30 breaths per minute, heart rate >=125 beats per minute, SpO2 less than or equal to (<=) 93% on room air at sea level or partial pressure of oxygen (PaO2)/fraction of inspired oxygen (FiO2) less than (<)300, heart rate >=125 beats per minute. (2) No criteria met for critical COVID-19

• Has either normal renal function or mild or moderate renal impairment: estimated creatinine clearance >30 milliliters per minute (mL/min) on Day 1

• Able to swallow the study drug (tablets)

• Men whose sexual partners are women of childbearing potential (WOCBP) must agree to comply with one of the following contraception requirements from the time of first dose of study medication (Day 1) until at least 30 days after the last dose of study medication: (a) Vasectomy with documentation of azoospermia. (b) Sexual abstinence. (c) Male condom plus partner use of one of the contraceptive

• WOCBP must agree to comply with one of the following contraception requirements from the time of first dose of study medication (Day 1) until at least 30 days after the last dose of study medication: (a) Sexual abstinence (b) Use of one of the contraceptive options (c) Vasectomy of male partner with documentation of azoospermia

Exclusion Criteria:

• The participant, in the opinion of the investigator, is not likely to survive for >=48 hours beyond Day 1

• Has a diagnosis of asymptomatic COVID-19, mild COVID-19, or critical COVID-19 on Day 1

• Has a documented current liver disease, or known hepatic or biliary abnormalities (with the exception of asymptomatic gallstones) at screening or on Day 1

• Has a Child Pugh score >= C

• Has a documented medical history of infection with human immunodeficiency virus or hepatitis A, B, or C at screening or on Day 1

• Has a documented active infection with tuberculosis at screening or on Day 1

• Has clinically significant ECG abnormalities at screening or on Day 1

• Requires dialysis or is on any renal replacement therapies at screening or on Day 1

• A female participant who is pregnant or planning to become pregnant during the study, breastfeeding, or has a positive pregnancy test at screening

• Receiving alpha-blockers, combined alpha/beta blockers, antihistamines, or any drugs that will affect the levels of cytokines released due to immune stress

• Has received any immunoglobulins within 6 months of screening or planned administration of any immunoglobulins during the screening and/or treatment periods

• Has a known history of drug abuse within 6 months of study start that would interfere with the participant's participation in the study

• Has a history of sensitivity to any of the study medications, or components thereof or a history of drug or other allergy that, in the opinion of the investigator or medical monitor, would contraindicate their participation

• Has participated in and/or plan to participate in another clinical study

• Will be transferred to another hospital which is not a study site within 72 hours

• Cannot read and speak either English or Spanish

Other protocol defined Inclusion/Exclusion criteria may apply

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Miami, Florida	Miami	Florida	United States	33155
2	Palms of Pasadena Hospital, Saint Petersburg, Florida	Saint Petersburg	Florida	United States	33707
3	Theia Clinical Research, St. Petersburg, Florida	Saint Petersburg	Florida	United States	33707
4	Idaho Falls, Idaho	Idaho Falls	Idaho	United States	83404
5	Winfield, Illinois	Winfield	Illinois	United States	60190
6	Butte, Montana	Butte	Montana	United States	59701
7	Tulsa, Oklahoma	Tulsa	Oklahoma	United States	74104
8	Kingsport, Tennessee	Kingsport	Tennessee	United States	37660
9	Amarillo, Texas	Amarillo	Texas	United States	79109
10	Mesquite, Texas	Mesquite	Texas	United States	75149

Sponsors and Collaborators

• FSD Pharma, Inc.

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: FSD Pharma, Inc.
• ClinicalTrials.gov Identifier: NCT04619706
• Other Study ID Numbers: FSD201-03
• First Posted: Nov 6, 2020
• Last Update Posted: Aug 24, 2022
• Last Verified: Apr 1, 2022

• Individual Participant Data (IPD) Sharing Statement: No
• Plan to Share IPD: No
• Studies a U.S. FDA-regulated Drug Product: Yes
• Studies a U.S. FDA-regulated Device Product: No
• Keywords provided by FSD Pharma, Inc.: SARS-CoV-2
• Additional relevant MeSH terms: COVID-19; Palmidrol

Study Results

No Results Posted as of Aug 24, 2022