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Placebo Device & Nasacort

Clayton Sleep Insititute · Phase 3 active Small molecule

Placebo Device & Nasacort is a Corticosteroid Small molecule drug developed by Clayton Sleep Insititute. It is currently in Phase 3 development for Seasonal allergic rhinitis, Perennial allergic rhinitis.

Nasacort is a corticosteroid that works by reducing inflammation in the nasal passages.

Nasacort is a corticosteroid that works by reducing inflammation in the nasal passages. Used for Seasonal allergic rhinitis, Perennial allergic rhinitis.

Likelihood of approval
58.3% vs 58.3% industry baseline
If approved by FDA: likely 2028–2030
Steps remaining: NDA/BLA submission
Confidence: High
Why this estimate
  • Baseline phase 3 → approval rate +58.3pp
    Industry-wide phase 3 drugs reach approval ~58.3% 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 2028–2030
EMA EU 2029–2031 +0.7 yr
MHRA GB 2029–2031 +0.7 yr
Health Canada CA 2029–2032 +0.9 yr
TGA AU 2029–2032 +1.2 yr
PMDA JP 2029–2032 +1.5 yr
NMPA CN 2030–2033 +2.3 yr
MFDS KR 2029–2032 +1.4 yr
CDSCO IN 2029–2033 +1.8 yr
ANVISA BR 2030–2033 +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 namePlacebo Device & Nasacort
SponsorClayton Sleep Insititute
Drug classCorticosteroid
ModalitySmall molecule
Therapeutic areaRespiratory
PhasePhase 3

Mechanism of action

It does this by inhibiting the release of inflammatory mediators from mast cells and other cells in the nasal mucosa, leading to a decrease in symptoms of allergic rhinitis.

Approved indications

Common side effects

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 Placebo Device & Nasacort

What is Placebo Device & Nasacort?

Placebo Device & Nasacort is a Corticosteroid drug developed by Clayton Sleep Insititute, indicated for Seasonal allergic rhinitis, Perennial allergic rhinitis.

How does Placebo Device & Nasacort work?

Nasacort is a corticosteroid that works by reducing inflammation in the nasal passages.

What is Placebo Device & Nasacort used for?

Placebo Device & Nasacort is indicated for Seasonal allergic rhinitis, Perennial allergic rhinitis.

Who makes Placebo Device & Nasacort?

Placebo Device & Nasacort is developed by Clayton Sleep Insititute (see full Clayton Sleep Insititute pipeline at /company/clayton-sleep-insititute).

What drug class is Placebo Device & Nasacort in?

Placebo Device & Nasacort belongs to the Corticosteroid class. See all Corticosteroid drugs at /class/corticosteroid.

What development phase is Placebo Device & Nasacort in?

Placebo Device & Nasacort is in Phase 3.

What are the side effects of Placebo Device & Nasacort?

Common side effects of Placebo Device & Nasacort include Nasal congestion, Headache, Nausea, Dizziness.

Related

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