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NCT Number: NCT02460588

Cyclophosphamide for Acute Exacerbation of Idiopathic Pulmonary Fibrosis

Acute exacerbation of idiopathic pulmonary fibrosis (AE-IPF) is a major event of IPF with an annual incidence between 5 and 10% and is responsible for the death of one third of IPF patients. When AE-IPF occurs, it is associated with poor survival with an overall mortality at 3 months upper of 50%. To date, no treatment has been proved to be effective in AE-IPF but the efficacy of cyclophosphamide (CYC) on survival has been suggested, mainly by retrospective series and needs to be confirmed. This confirmation is mandatory to improve prognosis of AE-IPF but also to avoid unsuspected deleterious effect as it as been shown with immunosuppressor in stable IPF.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Hôpital Tenon

Paris, France

About this study

Acute exacerbation of idiopathic pulmonary fibrosis (AE-IPF) is a major event of IPF with an annual incidence between 5 and 10% and is responsible for the death of one third of IPF patients. When AE-IPF occurs, it is associated with poor survival with an overall mortality at 3 months upper of 50%. To date, no treatment has been proved to be effective in AE-IPF but the efficacy of CYC on survival has been suggested, mainly by retrospective series and needs to be confirmed. This confirmation is mandatory to improve prognosis of AE-IPF but also to avoid unsuspected deleterious effect as it as been shown with immunosuppressor in stable IPF.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • ≥18 years of age
  • Definite or probable IPF diagnosis defined on 2011 international recommendations
  • Definite or suspicion of AE defined by IPFnet criteria after exclusion of alternative diagnosis of acute worsening.
  • Efficient contraceptive method within 1 month for women and 3 months for men after the last dose of treatment
  • Affiliation to the social security
  • Able to understand and sign a written informed consent form

Exclusion criteria

  • Identified etiology for acute worsening (i.e. infectious disease)
  • Known hypersensitivity or contra-indication to CYC or to any component of the study treatment
  • Patient on mechanical ventilation
  • Active bacterial, viral, fungal or parasitic infection
  • Active cancer
  • Patient on a lung transplantation waiting list
  • Treatment with CYC in the last 12 months
  • Patient participating to another clinical trial
  • Pregnancy or lactation

Treatment and study plan

Cyclophosphamide

Drug

Population is IPF patients with an AE who meet the inclusion and exclusion criteria defined below.

Intravenous Cyclophosphamide (CYC), 600 mg/m² (adapted to age and renal function, maximal dose of 1.2 g) at Day 0, Day 15, M1, M2

Placebo

Drug

Population is IPF patients with an AE who meet the inclusion and exclusion criteria defined below.

Other names: Control group

Corticosteroid (prednisolone)

Drug

All patients will receive non experimental medication with high dose of corticosteroid.

Other names: Both groups

Primary outcomes

  1. "Early" survival

    Time frame: 3 months

    All cause of mortality at 3 months

Secondary outcomes

  1. Overall Survival

    Time frame: 6 months and 12 montns

    Overall Survival at M6 and M12

  2. Respiratory disease-specific mortality

    Time frame: 6 months

    Respiratory disease-specific mortality at M3 and M6

  3. Respiratory Morbidity

    Time frame: 6 months

    \\Worsening dyspnea (0-100-mm visual analogue (VAS) scale anchored with 0 ''no breathlessness'' and 10 or 100 ''worst imaginable breathlessness". Worsening is defined an absolute decrease of 10 mm)

    • Or Increase need of supplemental oxygen of more than 3l/min to obtained a SaO2 > 90% or decrease of PaO2 of more than 10 mmHg with the same rate of flow supplemental oxygen
    • Or Decrease FVC of more than 10% of predicted value
    • Or Decrease diffuse capacity for carbon monoxide (DLCO) of more than 15% prednisolone
  4. Chest HRCT features (HRCT images will be scored at 5 levels)

    Time frame: 6 months

    Chest HRCT features at M3 and M6 compared to inclusion

  5. Prognosis factors of AE-IPF

    Time frame: 3 months

    PFTs results before AE-IPF

  6. Time to visit after clinical worsening

    Time frame: 3 months

  7. Laboratory evaluation (LDH, CRP) at AE diagnosis (composite)

    Time frame: 3 months

  8. Prognosis factors of AE-IPF

    Time frame: 3 months

    PaO2 at AE diagnosis

  9. Prognosis factors of AE-IPF

    Time frame: 3 months

    Chest HRCT features at AE diagnosis compared to HRCT before AE-IPF (if available)

  10. Prognosis factors of AE-IPF

    Time frame: 3 months

    Chest HRCT classification before AE-IPF (definite UIP, probable UIP, indeterminate), if available

  11. Time to dispense treatment of AE-IPF

    Time frame: 3 months

  12. Hemorrhagic cystitis (occurence of hematuria on urine dipstick and pelvic pain and/or dysuria should lead to cystoscopy)

    Time frame: 6 months

  13. Number of Infectious disease

    Time frame: 6 months

  14. Diabetes mellitus (capillary blood glucose monitoring and fasting plasma glucose > 1.26 g/l)

    Time frame: 6 months

  15. Hypertension (Blood pressure > 160/100 mmHg)

    Time frame: 6 months

  16. Clinical laboratory evaluation (blood count, serum creatinin measurement composite) according to Common Terminology Criteria for Adverse Event (CTCAE).

    Time frame: 6 months

Sponsors and collaborators

Lead sponsor

Assistance Publique - Hôpitaux de Paris

Other

Registry information

Official study title

Cyclophosphamide Added to Corticosteroid in the Treatment of Acute Exacerbation of Idiopathic Pulmonary Fibrosis: a Placebo-controlled Randomized Trial

Acronym: EXAFIP

Important dates

Study start
2015
Primary completion
2019
Study completion
2019
First posted
Jun 2, 2015
Registry last updated
Jun 30, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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