The KIN-FAST Trial (KIN001 For Accelerated Symptoms Termination) in Non Hospitalized Patients Infected With SARS-CoV-2

COVID-19 Clinical Trial

— KIN-FAST  

Official title:

The KIN-FAST Trial (KIN001 For Accelerated Symptoms Termination) A 4-week Double-blind, Randomized, Placebo-controlled, Phase II Study Evaluating the Effects of Oral Pamapimod 150 mg With Pioglitazone 10 mg Daily on COVID-19 Evolution and Recovery in Non-hospitalized Patients Infected With SARS-CoV-2 (Severe Acute Respiratory Syndrome-coronavirus-2)

Clinical Trial Details — Status: Suspended

Administrative data

• NCT number: NCT05659459
• Other study ID #: KIN001-204 - KIN-FAST
• Status: Suspended
• Phase: Phase 2
• Start date: August 25, 2022
• Est. completion date: October 31, 2025

Study information

• Verified date: October 2023
• Source: Kinarus AG
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Clinical trial on safety and efficacy of KIN001 in non-hospitalized patients with COVID-19.

Description:

This is a prospective, double-blind, randomized and placebo-controlled phase II trial to evaluate the safety and efficacy of KIN001 in non-hospitalized patients suffering from COVID-19. Randomization to one of two treatment arms (KIN001 versus Placebo) is at a ratio of 1:1.

Patients will receive treatment for 14 days and followed for another 14 days. The primary outcome is patient reported COVID-19 symptoms, using the FDA questionnaire developed for assessing COVID-19-related symptoms in outpatients.

The trial will be conducted in Switzerland and Germany.

Recruitment information / eligibility

• Status: Suspended
• Enrollment: 400
• Est. completion date: October 31, 2025
• Est. primary completion date: May 31, 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Diagnosis of symptomatic COVID-19 of less than 5 days' duration, with at least 1 point in at least 4 items of the symptom evaluation table, and at least 2 points in at least 2 items, OR a minimum total score of 6 points

2. Diagnosis of COVID-19 confirmed in the last 48 hours by a positive test for SARS-CoV-2 RNA by RT PCR or a rapid validated antigen test (excluding self-test), in a specimen from the upper respiratory tract, the saliva (antigen test), the lower respiratory tract or an expectorated sputum

3. No indication that the patient will be hospitalized in the next 48 hours for COVID-19 related reasons

4. Adult male or female patients aged = 18 years

5. Females must have a negative pregnancy test or must be post-menopausal

6. Able to understand and willing to sign an IRB/IEC approved written informed consent document.

7. Able to understand and be available for daily phone calls to evaluate symptoms.

Exclusion Criteria:

1. Patients with an indication for hospitalization (e.g. SpO2 <92%)

2. Patients participating in another clinical trial with a new investigational drug or investigational non-drug treatment

3. Known allergy or intolerance to pamapimod or any other ingredient of the IMP or another P38 inhibitor

4. Known allergy or intolerance of clinical relevance to pioglitazone or any other ingredient of the IMP.

5. Patients where oral administration of pioglitazone is contraindicated (i.e. cardiac failure or history of cardiac failure (NYHA stages I to IV), with hepatic impairment, diabetic ketoacidosis, current bladder cancer or a history of bladder cancer, uninvestigated macroscopic haematuria

6. Any use of CYP450 2C8 inducers (e.g. rifampicin)

7. Known or suspected active viral (including HIV, hepatitis B, hepatitis C), bacterial, mycobacterial or fungal infection other than COVID-19. Virologic testing not required unless infection is suspected.

8. Pregnant or breastfeeding women

9. Any uncontrolled concurrent illness that would put the patient at a greater risk or limit compliance with the study requirements as determined at the discretion of the investigator

10. Liver enzyme elevation more than 3x above normal in the last 4 weeks or at inclusion

11. Patients who are detained or committed to an institution by a law court or by legal authorities (subject is vulnerable, such as deprived of freedom)

Related Conditions & MeSH terms

• COVID-19

Intervention

Drug:
• KIN001
Oral tablet
• KIN001-Placebo
Comparator - Oral tablet with same appearance of KIN001

Locations

Country	Name	City	State
Germany	Praxis am Ebertsplatz	Cologne
Germany	Velocity Clinical Research Hamburg	Hamburg
Germany	Praxis am Neckar	Heidelberg
Switzerland	Hôpital de la Tour	Meyrin
Switzerland	Cabinet Dr Clément	Nyon
Switzerland	Cabinet Dr. Thanh	Nyon
Switzerland	Cabinet Dr. Dang	Onex
Switzerland	Cabinet Dr. Schaller	Onex

Sponsors (1)

Lead Sponsor	Collaborator
Kinarus AG

Countries where clinical trial is conducted

Germany,  Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Exploratory outcome - Sars-CoV-2 positive familiy members	Number of family members in the same household tested positive by Sars-CoV-2 PCR test two to 10 days after inclusion	10 days
Primary	COVID-19 symptoms evaluation	Number of days alive with no score > 1 in each of the symptoms and a maximum of 3 points in the total score*, measured from inclusion to day 28; *Assessing COVID-19-Related Symptoms in Outpatient Adult and Adolescent Subjects in Clinical Trials of Drugs and Biological Products for COVID-19 Prevention or Treatment Guidance for Industry https://www.fda.gov/drugs/guidance-compliance-regulatory-information/guidances-drugs	28 days
Secondary	COVID-19 time to recovery	Time to clinical recovery, based on patient-reported daily evaluation of symptoms, and defined as the number of days from start of administration of the investigational agent to the first of two consecutive days when any symptoms scored as 2 or 3 at study entry are scored as 0-1 AND any symptoms scored as 0-1 at study entry are scored as 0	28 days
Secondary	COVID-19 related hospital admissions	All-cause unplanned COVID-19 related hospital admissions	28 days
Secondary	Safety and tolerability assessing treatment emergent adverse events	Safety and tolerability of KIN001	28 days
Secondary	Total evaluation of COVID-10 symptoms score	Total sum of daily scores* of symptomes from inclusion to day 28; *Assessing COVID-19-Related Symptoms in Outpatient Adult and Adolescent Subjects in Clinical Trials of Drugs and Biological Products for COVID-19 Prevention or Treatment Guidance for Industry https://www.fda.gov/drugs/guidance-compliance-regulatory-information/guidances-drugs	28 days