1. Selection of donor according to the eligibility criteria

- Full medical history, concurrent medications, demographic data will be obtained.

- Complete clinical assessment with special emphasis on assessment of resolution of
symptoms

- Body weight, height.

- A confirmatory diagnostic test result (e.g., nasopharyngeal swab) at the time of
illness or serological test for SARS-CoV-2 antibodies after recovery will be
collected

- COVID -19 PCR test by nasopharyngeal swab.

- Complete blood count with differential counts

- Viral screening (HBV, HCV, HIV & Syphilis): Conventional testing by
chemiluminescence followed by nucleic acid testing (NAT)

- Donor's written consent

2. Plasma collection:

- Donor to be connected to microprocessor controlled plasmapheresis machine
containing single use disposable kit for every donor.

- A certain amount of blood is withdrawn by pump from the patient and immediately
anticoagulated then centrifuged in the machine.

- Blood components are separated into different layers according to the density of
each component.

- The plasma layer is collected and diverted into the collection bag while all other
components are infused back to the patient, thus ending the first cycle.

- Cycles are repeated until collecting a total of 400 ml of filtered plasma in the
collection bag; that is one complete therapeutic dose for one patient in need.

3. Pathogen reduction/Viral inactivation by the Solvent/Detergent (S/D) method:

- SD method is the gold standard for inactivation of enveloped viruses HBV, HCV and
HIV. All these viruses have a lipid outer coat enveloping the nucleic acid.

- Tri-N Butyl Phosphate (TNBP) acts as an organic solvent to remove lipids from the
membranes of pathogens.Tween-20 is a non-ionic detergent that stabilizes TNBP and
disrupts lipid bilayers, thus easing the extraction of lipids. Since the solvent is
toxic, it is removed using a sterile vegetable oil (Castor oil).

4. Measuring remnants of TNBP:

- By chromatography in Ain Shams Toxicology Center.

- Concentration should be less than 10 ppm.

5. Screening phase for patients selection:

• Obtaining informed consent: Written signed and dated informed consent will be obtained
from each patient before being entered into the study. The investigator, or a person
designated by the investigator, should fully inform the subject or, if the subject is
unable to provide informed consent, the subject's legally acceptable representative, of
all pertinent aspects of the trial. This will be obtained from each subject in
accordance with the recommendation of the revised Declaration of Helsinki. The
investigator will explain the nature, purpose and risks of the study. It will be clearly
stated that the patient is free to withdraw from the study at any time for any reason
without prejudice to future care, and with no obligation to give the reason for
withdrawal.

In case the patient is unable to provide his/her consent the legal guardian will give
verbal approval on behaves of the patient and after he he/she will be well informed by
the study design, procedure, risk and benefits over phone call.

If it is difficult to reach the legal guardian, emergency approval will be obtained by
Professional Legal Representative who will be the head authorities of the isolation
hospital.

- Full medical history, concurrent medications, demographic data will be obtained.

- A thorough physical examination will be performed.

- Body weight, height, BMI, vital signs (blood pressure, heart rate and temperature)
and Blood oxygen saturation) will be recorded.

- Chest x-ray and CT scan for chest will be recorded

- Ventilation parameters to be recorded if ventilated

- Laboratory to perform the following tests:

Complete blood count with differential counts, Renal function tests (RFTs) (serum
creatinine), Liver function tests (LFTs) (alanine amino transferase (ALT), aspartate
amino transferase (AST), total and direct bilirubin), Coagulation test; prothrombin time
and INR and D.dimer, HIV Ab, HCV Ab and HBV surface antigen (HBsAg), COVID -19 PCR test
by nasopharyngeal swab. Urine pregnancy test for females.

6. Treatment phase for eligible patients:

- Eligibility confirmed

- Treatment with collected plasma in a dose of 400 ml on single therapeutic dose on
Day1 as an add on therapy for the standard of care treatment (national guideline)
(Oseltamivir (150mg/12 hours for 5-10 days) and hydroxychroquine (400mg twice in
first day, 200 twice for 4-9 days) ± Azithromycin 500mg daily for 5 days.

- The patient's health status, and the presence of adverse events will be assessed
daily

- Complete physical examination will be performed daily.

- Vital signs (blood pressure, heart rate and temperature) will be recorded.

- Follow-up CXR will be performed on daily and /CT scan will be performed as
clinically indicated

- Coagulation test; prothrombin time and INR and D.dimer will be re-reassessed on day
3, 7, and 14

- HIV Ab, HCV Ab and HBV surface antigen (HBsAg) will be repeated at day 14

- COVID -19 PCR test by nasopharyngeal swab will be repeated every 72 hours.

- Post treatment period up to 30 days after end of treatment:

- Vital signs (blood pressure, heart rate and temperature) will be recorded.

- Symptoms and signs assessment will be done.