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PVC (twice weekly)

Wyeth is now a wholly owned subsidiary of Pfizer · Phase 3 active Small molecule Under review

PVC (twice weekly) is a Antiarrhythmic Small molecule drug developed by Wyeth is now a wholly owned subsidiary of Pfizer. It is currently in Phase 3 development for Prevention of recurrent symptomatic supraventricular tachycardia.

PVC works by blocking the action of certain electrical signals in the heart, helping to regulate its rhythm.

PVC, also known as Olopatadine, is a small molecule used in various medical studies, including those for Fecal Incontinence, Encopresis, and Oral Cancer. It has been studied in combination with traditional treatment, biofeedback, and electrical stimulation, but its exact mechanism of action is not specified in the provided information.

Likelihood of approval
59.3% 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).
  • Cardiovascular Phase 3 risk -2.0pp
    Modern cardiovascular outcome trials are large + long; many fail to beat aggressive standard-of-care.
  • Big-pharma sponsor +3.0pp
    Wyeth is now a wholly owned subsidiary of Pfizer 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 namePVC (twice weekly)
SponsorWyeth is now a wholly owned subsidiary of Pfizer
Drug classAntiarrhythmic
TargetAV node, bundle of His
ModalitySmall molecule
Therapeutic areaCardiovascular
PhasePhase 3

Mechanism of action

PVC achieves this by targeting the heart's electrical conduction system, specifically the atrioventricular (AV) node and the bundle of His. This helps to prevent abnormal heart rhythms and reduce the risk of complications such as stroke and heart failure.

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 PVC (twice weekly)

What is PVC (twice weekly)?

PVC (twice weekly) is a Antiarrhythmic drug developed by Wyeth is now a wholly owned subsidiary of Pfizer, indicated for Prevention of recurrent symptomatic supraventricular tachycardia.

How does PVC (twice weekly) work?

PVC works by blocking the action of certain electrical signals in the heart, helping to regulate its rhythm.

What is PVC (twice weekly) used for?

PVC (twice weekly) is indicated for Prevention of recurrent symptomatic supraventricular tachycardia.

Who makes PVC (twice weekly)?

PVC (twice weekly) is developed by Wyeth is now a wholly owned subsidiary of Pfizer (see full Wyeth is now a wholly owned subsidiary of Pfizer pipeline at /company/wyeth-is-now-a-wholly-owned-subsidiary-of-pfizer).

What drug class is PVC (twice weekly) in?

PVC (twice weekly) belongs to the Antiarrhythmic class. See all Antiarrhythmic drugs at /class/antiarrhythmic.

What development phase is PVC (twice weekly) in?

PVC (twice weekly) is in Phase 3.

What are the side effects of PVC (twice weekly)?

Common side effects of PVC (twice weekly) include Dizziness, Headache, Nausea, Fatigue.

What does PVC (twice weekly) target?

PVC (twice weekly) targets AV node, bundle of His and is a Antiarrhythmic.

Related

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