Study population: Patients with fibrotic lung sequelae after recovery from acute phase ofsevere COVID19 pneumonia Objectives: To evaluate the effect of pirfenidone administeredfor 24 weeks in patients who have pulmonary fibrotic changes after suffering severeCOVID19 pneumonia, analysed by - % change in forced vital capacity (FVC) - % fibrosis in high resolution computed tomography (HRCT) of the lung
Has been designed a clinical trial with an experimental and a control arm, with 2
experimental subjects per control (2:1), we will have to study 98 experimental subjects
and 50 control subjects, in total 148 patients. Randomization will be performed using a
centralized electronic system (IVRS) with 2: 1 randomized concealed assignment. This
randomization will be done by permuted blocks.
The study population will be patients with fibrosing lung sequelae after recovery from
severe COVID19 pneumonia.
This is a double-blind, masked, placebo-controlled clinical trial: the patient and the
investigator are unaware of the assigned treatment the patient receives.
Patients will follow a total of 5 clinic visits; V0 (screening, -1 days - +42 days from
signing the Informed Consent), V1 (randomization), V2 (week 12), V3 (week 24 or end of
treatment), V4 (week 28 or follow-up).
Visits Plan
- V0 - Screening: Initially, the informed consent will be collected. Subsequently, we
will proceed to collect clinical variables, blood tests and radiological
characteristics (chest CT scan; radiological signs of fibrosis such as tractional
bronchiolectasis, honeycombing, loss of lung volume and reticulation).
- V1 - Randomization: Before starting the drug:
Control analytics Serum pregnancy test for all women of childbearing age KBILD quality of
life test. This validated questionnaire will be completed by the patient following the
instructions of the staff.
Spirometry (CVF) and plethysmography (DLCO) TM6m. Extraction of blood for DNA isolation
(in those cases that have specifically signed the IC for genetics) and proteins (serum).
Once the screening evaluation has been completed, eligibility will depend on meeting the
inclusion criteria and not presenting any exclusion criteria. Those cases that are not
eligible will be informed and an adequate explanation will be provided.
- V2 - 12 weeks after starting medication. The patient's clinical status will be
collected
- V3 - 24 weeks (end of treatment period). Clinical data and quality of life test
(KBILD) will be collected, and chest CT scan, spirometry-plethysmography and TM6m
will be performed. Blood will be drawn for protein isolation (serum).
- V4 - 28 weeks (follow-up). Clinical and analytical variables will be collected.
Patients will have the telephone number of the main researcher or someone from the team
where they can call 24 hours, which will be specified on the patient's card (where it
will be identified that the patient participates in this study). In case of presenting
any problem or side effect in the period between visits, the patient will go to the
center and an additional visit will be made.
Study treatment:
Pirfenidone Name: Esbriet 267 mg hard capsules Dosage: 267 mg (capsules) Manufacturer:
Roche Pharma AG
Study drug administration schedule: The study medication will be started at incremental
doses, starting with 1602 mg / day (divided into three doses every 8 hours, 267 mg
capsules with each meal) and, if there is no liver or associated serious events, will be
increased on the 7th day to full doses of 2403 mg / day. The dose increase can be
extended for one more week if the investigator considers it safer (slight elevation of
liver enzymes, digestive discomfort or clear anorexia). Subsequently, 2403 mg / day will
be maintained (3 capsules in each meal during the day) except if it is necessary to
reduce the dose or suspend the drug due to adverse effects or associated problems (at the
discretion of the researcher).
Concomitant treatments prohibited:
The use of the following therapies is prohibited during study treatment:
- Cytotoxic, immunosuppressant, cytokine modulators, including but not limited to
azathioprine, bosentan, ambrisentan, cyclophosphamide, cyclosporine, etanercept,
iloprost, infliximab, leukotriene antagonists, methotrexate, high doses of
corticosteroids (more than 15 mg / day of prednisone or equivalent for more than 20
days), mycophenolate mofetil, tacrolimus, montelukast, tetrathiomolybdate, TNF-α
inhibitors, imatinib mesylate, interferon gamma-1b, and tyrosine kinase inhibitors.
- Strong CYP1A2 inhibitors (eg, Fluvoxamine, Enoxacin), P-glycoprotein inhibitors (eg,
Ketoconazole, erythromycin) or CYP3A4 (eg, Ketoconazole, erythromycin), or their
inducers (eg. Eg, rifampicin, carbamazepine, phenytoin).
- Any investigational therapy in an active clinical trial.
- Because moderate CYP1A2 inhibitors (eg, Ciprofloxacin) increase the systemic
exposure of pirfenidone (Esbriet® US label 2014), if ciprofloxacin is administered,
it should be limited to 250 or 500 mg daily (QD), and the patient should be closely
monitored.
Prohibited foods: The consumption of grapefruit juice will be prohibited during the
study.
Additional restriction: The use of any form of tobacco consumption will be prohibited.
Criteria for patient withdrawal from the study Participation in the study is voluntary
and the subjects can withdraw at any time without having to give explanations and without
this implying a detriment to the healthcare they receive in the future.
For her part, the researcher must withdraw a subject from the study:
- Adverse event or clinical situation of the patient that, in the clinical opinion,
makes it necessary to withdraw from the study. Patients can interrupt the medication
for up to 14 days, returning to the previous dose without requiring titration. If
they interrupt for more than 14 days, they have to gradually increase the dose. If
the patient cannot tolerate the minimum dose, then the treatment will be withdrawn,
allowing study visits to be completed.
- Request for withdrawal by the patient.
- Serious violation of protocol.
- Loss of follow-up.
- Pregnancy during the study. When a subject withdraws from the study, the
investigator will record the reason or reasons for withdrawal in the original
documents in the Medical Record.
End of clinical trial is defined as the date the last recruited patient completes the
last visit (LPLV). The last patient is expected to complete the last visit 4 weeks after
the last patient has completed treatment, which is expected to happen 14 months after the
start of the study.
Drug: Pirfenidone
Comparing the effect of pirfenidone in avoiding establishing or progression of fibrosis
induced after COVID19 infection
Drug: Placebo
Comparing the effect of pirfenidone in avoiding establishing or progression of fibrosis
induced after COVID19 infection
Inclusion Criteria:
- Age > 18 years
- Signed Informed Consent Form
- Ability to comply with the study protocol in the opinion of the Investigator
- Confirmation of SARS-COV2 infection in previous weeks (Confirmation of negativity or
no activity of SARS-COV2 before randomization using the usual tests performed in the
hospital), which induced severe pneumonia and ARDS, with subsequent torpid recovery
and/or incipient clinical-radiological signs of pulmonary fibrosis.
- HRCT with fibrotic radiological changes of at least 5% after recovery from the acute
process (HRCT chest during the screening period, performed minimum after 1 month of
the acute phase and maximum 90 days after hospital discharge)
- Be able to understand the information given and sign the informed consent
- For women or men of childbearing age who are not sterile, a commitment to use
non-hormonal contraception during the 24-week treatment period will be required.
Exclusion Criteria:
- Use of systemic steroids (oral or intravenous) at doses greater than 15 mg/day one
month prior to randomisation.
- Severe or moderate myopathy that may associate a decrease of FVC.
- Severe or life-limiting chronic disease prior to COVID19 infection, including severe
asthma, cancer, clinical dementia, IPF, or uncontrolled ischemic cardiomyopathy.
- Treatment with pirfenidone or nintedanib prior to Covid19
- Concomitant treatment with significant interactions with pirfenidone (such as
fluvoxamine).
- Participation in any other investigational trial throughout the study
- Active smoking.
- Relevant blood alterations in the analysis made during the screening period:
- Total bilirubin > 2 ULN
- AST/SGOT or ALT/SGPT > 2.5 ULN
- Alkaline phosphatase >3.0 ULN
- Creatinine Clearance <40 mL/min, calculated by the Cockcroft-Gault formula
- Pregnancy or lactation
- Concomitant treatments that can cause severe digestive problems.
- Gastric surgery in the last 3 months or similar procedures that may increase gastric
intolerance.
- Inability to complete required visits.
- Previous intolerance or allergy to pirfenidone or hypersensitivity to any of its
excipients.
- History of angioedema
University Hospital of Bellvitge
Hospitalet de Llobregat, Barcelona, Spain
Hospital Germans Trias i Pujol
Badalona, Spain
Hospital Clínic
Barcelona, Spain
Hospital del Mar
Barcelona, Spain
Hospital Sant Pau
Barcelona, Spain
Hospital La Princes
Madrid, Spain
Hospital Puerta de Hierro
Madrid, Spain
Hospital Ramón y Cajal
Madrid, Spain
Guadalupe Bermudo, MD, PhD
00342607689
ufip@bellvitgehospital.cat
Maria Molina-Molina, MD, PhD, Study Chair
Institut d'Investigació Biomèdica de Bellvitge