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Detox-B adjuvant

GlaxoSmithKline · Phase 3 active Biologic

Detox-B adjuvant is a Biologic drug developed by GlaxoSmithKline. It is currently in Phase 3 development for Vaccine adjuvant (indication under investigation in phase 3).

Detox-B adjuvant enhances immune response by promoting detoxification pathways and supporting innate immunity.

Detox-B adjuvant enhances immune response by promoting detoxification pathways and supporting innate immunity. Used for Vaccine adjuvant (indication under investigation in phase 3).

Likelihood of approval
62.3% 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).
  • Immunology slight uplift +1.0pp
    Mature endpoint landscape (ACR, DAS28, PASI) makes immunology approvals slightly more predictable.
  • Big-pharma sponsor +3.0pp
    GlaxoSmithKline is a top-20 pharma sponsor — historical approval rates run ~3pp above average due to scale, regulatory experience, and trial-design quality.
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 nameDetox-B adjuvant
SponsorGlaxoSmithKline
ModalityBiologic
Therapeutic areaImmunology
PhasePhase 3

Mechanism of action

As an adjuvant, Detox-B is designed to augment the body's natural detoxification mechanisms while simultaneously boosting immune activation. The exact molecular pathways remain proprietary, but adjuvants of this class typically work by activating pattern recognition receptors or enhancing antigen presentation to strengthen vaccine or immunotherapy efficacy.

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 Detox-B adjuvant

What is Detox-B adjuvant?

Detox-B adjuvant is a Biologic drug developed by GlaxoSmithKline, indicated for Vaccine adjuvant (indication under investigation in phase 3).

How does Detox-B adjuvant work?

Detox-B adjuvant enhances immune response by promoting detoxification pathways and supporting innate immunity.

What is Detox-B adjuvant used for?

Detox-B adjuvant is indicated for Vaccine adjuvant (indication under investigation in phase 3).

Who makes Detox-B adjuvant?

Detox-B adjuvant is developed by GlaxoSmithKline (see full GlaxoSmithKline pipeline at /company/gsk).

What development phase is Detox-B adjuvant in?

Detox-B adjuvant is in Phase 3.

Related

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