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Placebo (PBO)

Ridgeback Biotherapeutics, LP · Phase 3 active Small molecule

Placebo (PBO) is a Small molecule drug developed by Ridgeback Biotherapeutics, LP. It is currently in Phase 3 development for Control arm in phase 3 clinical trials (specific indication depends on the active comparator).

Placebo has no active pharmacological mechanism; it is an inert substance used as a control in clinical trials.

Placebo has no active pharmacological mechanism; it is an inert substance used as a control in clinical trials. Used for Control arm in phase 3 clinical trials (specific indication depends on the active comparator).

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 (PBO)
SponsorRidgeback Biotherapeutics, LP
ModalitySmall molecule
PhasePhase 3

Mechanism of action

Placebo is a non-therapeutic control agent administered in blinded clinical trials to establish baseline efficacy and safety profiles of investigational drugs. Any observed effects are attributable to the placebo effect—psychological and physiological responses to the expectation of treatment rather than pharmacological action. Placebos are essential for determining whether observed clinical benefits exceed those from natural disease progression or psychological factors.

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 Placebo (PBO)

What is Placebo (PBO)?

Placebo (PBO) is a Small molecule drug developed by Ridgeback Biotherapeutics, LP, indicated for Control arm in phase 3 clinical trials (specific indication depends on the active comparator).

How does Placebo (PBO) work?

Placebo has no active pharmacological mechanism; it is an inert substance used as a control in clinical trials.

What is Placebo (PBO) used for?

Placebo (PBO) is indicated for Control arm in phase 3 clinical trials (specific indication depends on the active comparator).

Who makes Placebo (PBO)?

Placebo (PBO) is developed by Ridgeback Biotherapeutics, LP (see full Ridgeback Biotherapeutics, LP pipeline at /company/ridgeback-biotherapeutics-lp).

What development phase is Placebo (PBO) in?

Placebo (PBO) is in Phase 3.

Related

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