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AZN — AstraZeneca PLC

AZN (AstraZeneca PLC) stock: $186.42, $289.09B market cap, $5.71B cash, $313.00B EV, $289.12B fully diluted market cap. Lead program: olaparib (Metastatic Castration-resistant Prostate Cancer), Phase 4. Data from Fully Diluted's biotech stocks database.

What they do

The Company’s registered number is 2723534 and its registered office is at 1 Francis Crick Avenue, Cambridge Biomedical Campus, Cambridge CB2 0AA, United Kingdom (Tel: +44 20 3749 5000). From February 1993 until April 1999, the Company was called Zeneca Group PLC.

Source: 20-F FY2025 via SEC EDGAR

Share price
$186.42
Market cap
$289,086.3M
Cash
$5,711.0M
Enterprise value
$312,997.3M

Balance sheet

Cash$5,711.0M
Debt$29,622.0M
Net cash-$23,911.0M
Enterprise value$312,997.3M
Basic shares1,550.7M shares
Fully diluted shares1,550.9M shares
Fully diluted market cap$289,120.3M
Cash per share$3.68
Quarterly burn+$3,738.0M generated

Cash figures as of 2025-12-31. Database snapshot: 2026-11-07.

Share structure

Common
1,550.9M
Pre-funded warrants
—
Options
—
RSUs
—
Warrants
—
Converts
—
Conv preferred
—
ESPP reserve
—
FDSO
1,550.9M

Cap table as of 2025-12-31.

Price history

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Next catalyst

Durvalumab · Now - Nov 7, 2026 Now · Phase 2 · Early Small (cT1N0) Triple Negative Breast Cancer

Recently reported

Tezepelumab Phase 3 Positive · 2026-10-20
Primary: Co-primary endpoints at Week 24 in CROSSING (NCT05583227): histologic remission (peak eosinophil count <=6 per high power field) and change in Dysphagia Symptom Questionnaire (DSQ) score — Histologic remission 64.8% (tezepelumab 210 mg) and 68.9% (420 mg) vs 3.5% placebo (p<0.001 for both); LS mean DSQ change -18.8 points (210 mg; p=0.049) and -22.0 points (420 mg; p<0.001) vs -14.7 placebo
· 368 patients aged 12-80 randomized 1:1:1 to tezepelumab 210 mg, 420 mg, or placebo every four weeks
· Week 52 histologic remission 67.8% (210 mg) and 63.3% (420 mg) vs 5.4% placebo (p<0.001)
· Week 52 DSQ change -22.1 and -24.0 vs -13.2 placebo (p<0.001)
· Total endoscopic remission (EREFS=0) at Week 52: 34.4% (210 mg) and 29.5% (420 mg) vs 4.1% placebo (p<0.001)
· First published numeric results; topline was first announced qualitatively on August 27, 2026
Safety: Safety profile consistent with approved indications; most frequent adverse events were upper respiratory infection (nasopharyngitis), headache and diarrhea
Source release →
efzimfotase Phase 3 Missed primary · 2026-10-11
HICKORY Phase 3 · hypophosphatasia
Source release →
Durvalumab Phase 3 Positive · 2026-09-25
Source release →
tozorakimab Phase 3 Positive · 2026-09-08
OBERON · COPD
Source release →
tozorakimab Phase 3 Positive · 2026-09-08
TITANIA · COPD
Source release →
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