The purpose of this clinical trial is to evaluate the safety and tolerability of twodoses (dose A and dose B) of Standardized Conditioned Medium Obtained by Coculture ofMonocytes and Mesenchymal Stromal Cells (PRS CK STORM) in the prevention ofCOVID-19-associated cytokine storm in participants with a confirmed diagnosis ofSARS-CoV-2 infection, recently hospitalized (less than 3 days) and who have had symptomsfor up to a maximum of 10 days prior to screening.The main questions it aims to answer are: - Are both doses of PRS CK STORM (dose A and dose B) safe as an intravenous drug to prevent and treat inflammatory processes, such as the cytokine storm associated with severe infectious processes, including COVID-19? - Are both doses of PRS CK STORM (dose A and dose B) effective as an intravenous drug to prevent COVID-19 associated cytokine storm compared to the control group? - What are the anti-inflammatory and pro-inflammatory cytokine profiles after treatment with two different doses of PRS CK STORM in participants hospitalized for COVID-19 classified with mild disease severity according to the World Health Organization (WHO) Clinical Progression Scale?Researchers will compare both doses of PRS CK STORM with the control group to testwhether the anti-inflammatory action of PRS CK STORM is safe and effective in treatinginflammatory processes, such as the cytokine storm associated with severe infectiousprocesses, including COVID-19. In addition, the anti-inflammatory and pro-inflammatorycytokine profiles after treatment PRS CK STORM compared to placebo group in COVID-19participants will be also studied.
This is a double-blind, randomized, phase I/II pilot trial study of two doses of PRS CK
STORM in hospitalized adult participants with confirmed SARS-CoV-2 infection by RT-PCR.
All participants will receive the standard of care for SARS-CoV-2 infection as described
in the COVID-19 Patient Management Protocol. Participants who meet the eligibility
criteria will be randomized in blocks to reach the 2:2:1 ratio (dose A: dose B: placebo).
This study consists of two parts:
Part 1: Two different doses (A and B) of PRS CK STORM will be evaluated in 2 groups of 4
participants (3:1; PRS CK STORM: placebo). It starts with a first sentinel group of 4
participants who will be assigned to placebo or study drug dose A. First, only 2
participants will randomly be assigned to receive the active treatment of dose A or
placebo for 5 consecutive days. These 2 first participants will be followed up to 48h
after the last drug administration (short-term safety follow-up period) when a safety
assessment will be completed before treating the other 2 participants in this group.
If the study drug is considered safe during the short-term safety assessment planned 48h
after the last drug administration, then 2 additional participants will be treated with
dose A for 5 consecutive days to complete the first sentinel group of 4 participants.
These 2 participants will be followed up to 48h after the last study drug administration
before moving to dose B.
After the assessment of data collected follow-up for this first group, a second small
sentinel group of other 4 participants will be treated with a higher dosage (dose B)
following the same process: firstly, only 2 participants will randomly receive the active
treatment of dose B or placebo for 5 consecutive days and then these 2 first participants
will be followed up to 48h after.
If the study drug is considered safe during the safety assessment planned 48h after last
drug administration, then two additional participants will be treated with dose B for 5
consecutive days to complete the sentinel second group of 4 participants evaluating dose
B. These 2 participants will be also followed up to 48h after the last study drug
administration before moving to Part 2.
All these 8 participants included in Part 1 will continue in a long-term safety follow-up
period until 1 year post treatment.
Part 2: 42 additional participants will be treated for 5 consecutive days. These 42
participants will be randomized to three treatment arms: 17 in the active arm with dose
A, 17 participants in the active arm with dose B and 8 participants in the placebo arm.
All participants in Part 2 will be followed up to 48h after the last study drug
(short-term safety follow-up period). Once all participants treated in Part 2 finished
the short-term safety follow-up period (48h after last study drug administration), all
data will be verified and statistically analyzed in an interim analysis. All participants
will be followed up to 1 year post treatment (long-term safety follow-up period).
Therefore, considering the participants enrolled in Part 1 and Part 2 the total number of
participants for safety, tolerability and efficacy analysis will be 50 assigned to three
different arms (total randomization ratio 2:2:1), 20 participants will receive dose A, 20
participants will receive dose B and 10 participants will receive placebo.
To sum up, considering the participants enrolled in Part 1 and Part 2 the total number of
participants for safety, tolerability and efficacy analysis will be 50 assigned to three
different arms (total randomization ratio 2:2:1), 20 participants will receive dose A of
PRS CK STORM, 20 participants will receive dose B of PRS CK STORM and 10 participants
will receive placebo.
The estimated duration of the study for individual participants will be 12 months
(screening: 3 days, treatment period: 5 days, short-term safety follow-up period: 2 days
after the last drug intake and long-term safety follow-up period: up to 48 weeks from
randomization).
It is hypothesized that both doses of PRS CK STORM for intravenous administration are
safe, well tolerated and clinically beneficial versus placebo for participants with
COVID-19-associated cytokine storm.
Drug: Placebo comparator
A single dose of saline solution 0.9% for infusion
Other Name: Saline Solution
Drug: PRS CK STORM
A single dose of PRS CK STORM (dose A) for infusion
Drug: PRS CK STORM
A single dose of PRS CK STORM (dose B) for infusion.
Inclusion Criteria:
1. Signed informed consent by the patient or legal representative prior to the
initiation of any study-specific procedure.
2. Males and females with a confirmed diagnosis of SARS-CoV-2 infection by positive
Reverse Transcription Polymerase Chain Reaction (RT-PCR).
3. Age more than 18 years old at the time of the consent.
4. Participants to be hospitalized or who have been admitted for less than 3 days with
a positive RT-PCR result and who have had symptoms up to a maximum of 10 days prior
to screening.
5. Female participants must be, either surgically sterilized or at least 1 year
postmenopausal (confirmed by follicle-stimulating hormone [FSH] more than 20
international units [Ius] only for women under 54) or using adequate birth control
(hormonal contraception, intrauterine contraceptive device, double barrier methods
[condom with spermicide, diaphragm with spermicide, or condom and diaphragm]) or
sexual abstinence for up to 90 days after the last treatment administration. Male
participants must be willing to use barrier contraception (condom) for up to 90 days
after the last treatment administration.
6. Participants classified in 4 or 5 score of severity according to WHO clinical
progression scale:
Level 4: hospitalized, no oxygen therapy. Level 5: hospitalized, oxygen by mask or nasal
prongs.
Exclusion Criteria:
1. Failure to perform screening or baseline examinations.
2. Body Mass Index (BMI) more than or equal to 35.
3. Not confirmed SARS-CoV-2 infection by RT-PCR.
4. Participants who have been previously classified in a higher score than 5 in WHO
clinical progression scale
5. Clinically significant, advanced or unstable disease that may interfere with primary
or secondary variable evaluations, may bias the clinical assessment, such as:
1. Liver function test abnormalities or other signs of hepatic insufficiency:
Aspartate transaminase (AST), alanine transaminase (ALT) more than 3 per upper
limit of the reference range, total bilirubin more than or equal to 2 mg/dL;
except for subjects with isolated elevation of indirect bilirubin relating to
Gilbert syndrome.
2. Renal insufficiency (serum creatinine more than 2 mg/dL (more than 150 μmol/L)
and creatinine clearance less than 60 (according to Cockcroft-Gault formula).
3. Myocardial infarction, unstable angina, heart failure within 3 months before
screening.
4. Bradycardia (heartbeat less than 50/min).
5. Atrioventricular block (type II / Mobitz II and type III), congenital long QT
syndrome, sinus node dysfunction or prolonged QTcF interval (males more than
450 msec and females more than 470 msec using Fridericia's formula: QTc = QT/
RR^2 ).
6. Uncontrolled diabetes mellitus (blood glucose level above 500 mg/dL) at the
time of admission.
7. Malignant tumors within the last 5 years except skin malignancies (other than
melanoma) or indolent prostate cancer
8. Metastases.
9. Human Immunodeficiency Virus (HIV), HBV [hepatitis B surface antigen (HBs Ag)
positive (+), or detected sensitivity on the HBV deoxyribonucleic acid (DNA),
polymerase chain reaction (PCR) qualitative test for hepatitis B core antibody
(HBc Ab) positive subjects] or HCV [HCV ribonucleic acid (RNA) detectable in
any subject with positive anti-HCV antibody (HCV Ab)].
10. Other serious active viral infections apart from SARS-CoV-2 that are requiring
specific antimicrobial treatment.
6. Inability to comply with the study and monitoring procedures.
7. Pregnant and breastfeeding females (pregnancy test positive).
8. Suspected or known history of drug or alcohol abuse.
9. Enrollment in another investigational drug study within 1 month before the screening
10. Subject who has any condition, including any psychological or psychiatric condition,
in the opinion of the Investigator, would compromise the safety of the subject or
the quality of the data and renders the subject an unsuitable candidate for the
study.
Hospital Universitario de Fuenlabrada
Fuenlabrada, Madrid, Spain
Investigator: Juan Victor San Martin Lopez, Dr
Pedro Lapuente, Dr.
+ 34 661976328
p.lapuente@peaches.es
Juan Carlos de Gregorio
+34 607964152
jcg@peaches.es