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Viviant
Viviant is a Small molecule drug developed by Pfizer. It is currently in Phase 2 development.
Viviant, also known as conjugated estrogens/bazedoxifene (CE/BZA), is a medication used to treat postmenopause, menopause, prediabetes, obesity, and osteoporosis. It is a combination of conjugated estrogens and bazedoxifene, which is an estrogen receptor modulator.
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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). -
Big-pharma sponsor
+3.0pp
Pfizer is a top-20 pharma sponsor — historical approval rates run ~3pp above average due to scale, regulatory experience, and trial-design quality.
| 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 | Viviant |
|---|---|
| Sponsor | Pfizer |
| Modality | Small molecule |
| Therapeutic area | Other |
| Phase | Phase 2 |
Approved indications
Common side effects
Key clinical trials
- Pilot Study of Bazedoxifene Plus Conjugated Estrogen on Imaging and Blood Biomarkers (EARLY_PHASE1)
- Phase IIB Trial of Bazedoxifene Plus Conjugated Estrogens (PHASE2)
- Bazedoxifene Acetate as a Remyelinating Agent in Multiple Sclerosis (PHASE2)
- Raising Insulin Sensitivity in Post Menopause (EARLY_PHASE1)
- The PROMISE Study: Duavee in Women With DCIS (PHASE2)
- Advancing Postmenopausal Preventive Therapy (PHASE2)
- Affect of Duavive on Mood & Anxiety Symptoms (PHASE1)
- Endometriosis and Microvascular Dysfunction; Simvastatin and Duavee (PHASE4)
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:
- Viviant CI brief — competitive landscape report
- Viviant updates RSS · CI watch RSS
- Pfizer portfolio CI
Frequently asked questions about Viviant
What is Viviant?
Who makes Viviant?
What development phase is Viviant in?
Related
- Manufacturer: Pfizer — full pipeline
- Therapeutic area: All drugs in Other
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing