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Catalyst Dossier · compiled by CeliA 🧫

Galderma Group AG/ADR (GDERF)

Biotechnology · market cap $48.7B · as of 2026-07-09

Research and calibrated estimates, not financial advice — verify before acting.

Next catalyst
2026-12-15 (est.)
Phase 2
Pipeline
10
programs
Upcoming events
1
next 90d+
Dossier
Ready
cached
Non-US-listed company. Financial statements and forensic scores here come from US SEC filings (10-K/10-Q), which foreign issuers don’t file — those sections may be blank. The catalyst calendar, pipeline, approval odds, price context and (where covered) analyst targets still apply.
Galderma Group AG (GDERF) is a dermatology-focused company with a market cap of approximately $48.7B, operating across aesthetics, dermatological therapeutics, and dermocosmetics. Its pipeline spans multiple Phase 2 and Phase 3 programs including botulinum toxin neuromodulators, nemolizumab for atopic dermatitis, and CD07805/47 gel for rosacea, positioning it as a broad-spectrum dermatology platform rather than a single-asset bet.
The catalyst path
  • 2026-12-15 (est.)Phase 2 · Nemolizumabimp 7/10
Pipeline
AssetPhaseIndication
botulinum toxinPhase 3Lateral Canthal Lines
NemolizumabPhase 3Moderate-to-Severe Atopic Dermatitis
Botulinum Toxin Type APhase 2Glabellar Frown Lines
Metvix® creamPhase 3Basal Cell Carcinoma
AdapalenePhase 2Acne Scars
CD 2027Phase 2Plaque-type Psoriasis
botulinum toxin neuromodulatorPhase 3Glabellar Frown Lines (GL)
CD07805/47 gelPhase 3Rosacea
QM1114-DPPhase 3Glabellar Frown Lines
clobetasol propionate shampoo (2/week)Phase 3Scalp Seborrheic Dermatitis

The full dossier is a Pro feature

Thesis, bull & bear, the if-approved scenario, financials, smart-money signals and risks — compiled by CeliA. The catalyst path & pipeline above are free.

Sources & data
  • SEC filings EDGAR filings for GDERF (10-K, 10-Q, S-3, 13D/G, Form 4)
  • Clinical trials 10 registered trials on ClinicalTrials.gov (per-trial NCT links in the pipeline)
  • Market & financial data Financial Modeling Prep / financialdata.net — prices, statements, key metrics, insider & institutional filings.
  • Regulatory openFDA, FDA advisory & PDUFA calendars.

Approval odds use historical phase base rates; the if-approved scenario is illustrative (see its note). Figures trace to the sources above — verify before acting.

Data from CatalystAlert (ClinicalTrials.gov, SEC EDGAR, openFDA, Financial Modeling Prep). Compiled by CeliA. Not financial advice.