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Bronchial fibroscopy

CMC Ambroise Paré · Phase 2 active Biologic ✓ Verified May 2026

Bronchial fibroscopy is a Biologic drug developed by CMC Ambroise Paré. It is currently in Phase 2 development for Diagnosis of respiratory diseases such as chronic obstructive pulmonary disease (COPD), asthma, and lung cancer.

Bronchial fibroscopy is a diagnostic procedure that uses a flexible tube with a camera and light to visually examine the airways and lungs.

Bronchial fibroscopy is a medical procedure used to study conditions such as chronic obstructive pulmonary disease (COPD), severe asthma, and asthma in children. It involves the use of a bronchoscope to examine the airways, and has been used in conjunction with interventions such as sitaxentan, a muscarinic acetylcholine receptor M3 agonist, in clinical trials.

Likelihood of approval
15.3% vs 15.3% industry baseline
If approved by FDA: likely 2031–2034
Steps remaining: Phase 3 → NDA/BLA submission
Confidence: Medium
Why this estimate
  • Baseline phase 2 → approval rate +15.3pp
    Industry-wide phase 2 drugs reach approval ~15.3% of the time (BIO/Informa 2023 industry benchmark across all therapeutic areas).
Predicted approval windows by jurisdiction (conditional on FDA approval)
Regulator Country Likely year Lag vs FDA
FDA US 2031–2034
EMA EU 2032–2035 +0.7 yr
MHRA GB 2032–2035 +0.7 yr
Health Canada CA 2032–2036 +0.9 yr
TGA AU 2032–2036 +1.2 yr
PMDA JP 2032–2036 +1.5 yr
NMPA CN 2033–2037 +2.3 yr
MFDS KR 2032–2036 +1.4 yr
CDSCO IN 2032–2037 +1.8 yr
ANVISA BR 2033–2037 +2.3 yr

Hover any row for the lag rationale. Lag estimates are reduced when the drug has FDA Breakthrough or EMA PRIME designation (sponsors file globally in parallel).

Estimate based on the BIO/Informa industry phase transition rates plus per-drug modifiers for therapeutic area, sponsor type, FDA designations, mechanism, and trial design. Per-jurisdiction lags from Tufts CSDD international approval studies. Not investment, clinical or regulatory advice. Methodology: /methodology#likelihood.

At a glance

Generic nameBronchial fibroscopy
SponsorCMC Ambroise Paré
ModalityBiologic
Therapeutic areaRespiratory
PhasePhase 2

Mechanism of action

The procedure involves inserting the flexible tube through the nose or mouth and guiding it through the airways to the lungs. This allows for the examination of the airway walls, bronchial tubes, and lung tissue for signs of disease or damage.

Approved indications

Common side effects

No common side effects on file.

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:

Frequently asked questions about Bronchial fibroscopy

What is Bronchial fibroscopy?

Bronchial fibroscopy is a Biologic drug developed by CMC Ambroise Paré, indicated for Diagnosis of respiratory diseases such as chronic obstructive pulmonary disease (COPD), asthma, and lung cancer.

How does Bronchial fibroscopy work?

Bronchial fibroscopy is a diagnostic procedure that uses a flexible tube with a camera and light to visually examine the airways and lungs.

What is Bronchial fibroscopy used for?

Bronchial fibroscopy is indicated for Diagnosis of respiratory diseases such as chronic obstructive pulmonary disease (COPD), asthma, and lung cancer.

Who makes Bronchial fibroscopy?

Bronchial fibroscopy is developed by CMC Ambroise Paré (see full CMC Ambroise Paré pipeline at /company/cmc-ambroise-par).

What development phase is Bronchial fibroscopy in?

Bronchial fibroscopy is in Phase 2.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing