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CHINIOFON
CHINIOFON is a chiniofon drug. It is currently in Phase 2 development.
CHINIOFON is thought to work by interacting with a specific biological target, but the exact mechanism is not well understood.
CHINIOFON is a small molecule drug in the chiniofon class, but information on its target, approved indications, and commercial status is limited. Its mechanism of action and pharmacokinetic properties are not well-documented. As a result, it is difficult to provide a comprehensive summary of CHINIOFON's characteristics and clinical use. Further research is needed to understand its potential applications and safety profile. Unfortunately, there is not enough information available to provide a detailed summary.
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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).
| 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 name | CHINIOFON |
|---|---|
| Drug class | chiniofon |
| Target | Catechol O-methyltransferase |
| Modality | Small molecule |
| Therapeutic area | Other |
| Phase | Phase 2 |
Mechanism of action
Imagine CHINIOFON as a key that fits into a lock in the body. When it binds to the lock, it can either turn the key (activating a response) or block the key from turning (inhibiting a response). However, the specific lock and key interaction for CHINIOFON is not well-documented.
Approved indications
Common side effects
Key clinical trials
- Lung Disease and Its Affect on the Work of White Blood Cells in the Lungs
- Secondhand Smoke Respiratory Health Study (PHASE4)
- Effects of Oral Doxofylline and Procaterol on Chronic Obstructive Pulmonary Disease (PHASE4)
- Add-on Clioquinol in Drug-resistant Childhood Epilepsy: an Exploratory Study (PHASE2)
- Assessing the Efficacy of CREWS01 to Decrease Usage of Rescue Inhalers in Moderate to Severe Asthmatic Adults (PHASE2)
- Comparison of Single-Dose Efficacy of an Albuterol Breath-Actuated Inhaler (Albuterol-HFA-BAI) Versus an Albuterol Metered-Dose Inhaler (Albuterol-HFA-MDI) in Participants With Asthma (PHASE4)
- Study to Evaluate the Safety of Sebryl® and Sebryl Plus® in Seborrheic Dermatitis and Psoriasis of Scalp
- Efficacy and Safety Comparison of Albuterol Spiromax® and ProAir® Hydrofluoroalkane (HFA) in Pediatric Patients (PHASE2)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial 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:
- CHINIOFON CI brief — competitive landscape report
- CHINIOFON updates RSS · CI watch RSS
Frequently asked questions about CHINIOFON
What is CHINIOFON?
How does CHINIOFON work?
What drug class is CHINIOFON in?
What development phase is CHINIOFON in?
What does CHINIOFON target?
Related
- Drug class: All chiniofon drugs
- Target: All drugs targeting Catechol O-methyltransferase
- Therapeutic area: All drugs in Other
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing