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Cimicifuga Herbarium

Phytopharm Consulting Brazil · Phase 3 active Small molecule

Cimicifuga Herbarium is a Herbal extract / phytoestrogen Small molecule drug developed by Phytopharm Consulting Brazil. It is currently in Phase 3 development for Menopausal vasomotor symptoms (hot flashes, night sweats).

Cimicifuga (black cohosh) herbarium extract modulates estrogen receptor signaling and reduces vasomotor symptoms through phytoestrogen activity.

Cimicifuga (black cohosh) herbarium extract modulates estrogen receptor signaling and reduces vasomotor symptoms through phytoestrogen activity. Used for Menopausal vasomotor symptoms (hot flashes, night sweats).

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 nameCimicifuga Herbarium
SponsorPhytopharm Consulting Brazil
Drug classHerbal extract / phytoestrogen
ModalitySmall molecule
Therapeutic areaWomen's Health / Menopause
PhasePhase 3

Mechanism of action

Cimicifuga contains triterpene glycosides and other phytochemicals that interact with estrogen receptors and serotonin pathways, reducing hot flashes and night sweats associated with menopause. The mechanism involves both direct estrogenic effects and modulation of thermoregulatory centers in the hypothalamus.

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 Cimicifuga Herbarium

What is Cimicifuga Herbarium?

Cimicifuga Herbarium is a Herbal extract / phytoestrogen drug developed by Phytopharm Consulting Brazil, indicated for Menopausal vasomotor symptoms (hot flashes, night sweats).

How does Cimicifuga Herbarium work?

Cimicifuga (black cohosh) herbarium extract modulates estrogen receptor signaling and reduces vasomotor symptoms through phytoestrogen activity.

What is Cimicifuga Herbarium used for?

Cimicifuga Herbarium is indicated for Menopausal vasomotor symptoms (hot flashes, night sweats).

Who makes Cimicifuga Herbarium?

Cimicifuga Herbarium is developed by Phytopharm Consulting Brazil (see full Phytopharm Consulting Brazil pipeline at /company/phytopharm-consulting-brazil).

What drug class is Cimicifuga Herbarium in?

Cimicifuga Herbarium belongs to the Herbal extract / phytoestrogen class. See all Herbal extract / phytoestrogen drugs at /class/herbal-extract-phytoestrogen.

What development phase is Cimicifuga Herbarium in?

Cimicifuga Herbarium is in Phase 3.

What are the side effects of Cimicifuga Herbarium?

Common side effects of Cimicifuga Herbarium include Gastrointestinal upset, Headache, Dizziness, Rash.

Related

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