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BNTC — Benitec Biopharma Inc.

BNTC (Benitec Biopharma Inc.) stock: $9.25, $322.5M market cap, $180.0M cash, $142.5M EV, $568.6M fully diluted market cap. Next expected readout: Nov-30. Lead program: BB-301: Dose escalation phase 1b cohort 1 (Oculopharyngeal Muscular Dystrophy), Phase 2. Data from Fully Diluted's biotech stocks database.

What they do

We are developing a silence and replace-based therapeutic (BB-301) for the treatment of Oculopharyngeal Muscular Dystrophy ("OPMD"), a chronic, life-threatening genetic disorder. BB-301 is an AAV-based gene therapy designed to permanently silence the expression of the disease-causing gene (to slow, or halt, the biological mechanisms underlying disease progression in OPMD) and to simultaneously replace the mutant gene with a functional gene (to drive restoration of function in diseased cells).

Source: 10-K FY2026 via SEC EDGAR

Share price
$9.25
Market cap
$322.5M
Cash
$180.0M
Enterprise value
$142.5M

Balance sheet

Cash$180.0M
Debt$0.0M
Net cash$180.0M
Enterprise value$142.5M
Basic shares34.4M shares
Fully diluted shares61.5M shares
Fully diluted market cap$568.6M
Cash per share$5.23
Quarterly burn$4.9M
Cash runway36.4 quarters

Cash figures as of 2026-06-30. Database snapshot: 2026-11-10.

Share structure

Common
34.4M
Pre-funded warrants
15.1M
Options
7.0M
RSUs
0.0M
Warrants
4.9M
Converts
0.0M
Conv preferred
0.0M
ESPP reserve
0.0M
FDSO
61.5M

Cap table as of 2026-06-30.

Price history

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Next catalyst

BB-301 · Est. Jul 16, 2027 · guidance midpoint · guided in 7 mo

Recently reported

BB-301: Dose escalation phase 1b cohort 1 Phase 1 Positive · 2026-10-28
BB-301 · oculopharyngeal muscular dystrophy
Primary: Responder status and swallowing function in the Phase 1b/2a study (throat emptying ability by videofluoroscopic evaluation of post-swallow food and liquid residue, functional swallowing capacity by Cold-Water Timed Drinking Test, total Sydney Swallow Questionnaire score, and throat closing ability) — 100% response rate observed across all Patients treated to date (all six Cohort 1 low-dose patients and all three Cohort 2 high-dose patients are formal Responders to BB-301)
· Cohort 1: 12-month post-treatment follow-up results for all six patients; Cohort 2: 9-month follow-up for the first patient and 3-month follow-up for the second and third patients
· At 3 months post-treatment, 67% of Cohort 1 and 100% of Cohort 2 patients met the statistical criteria for response for improved throat emptying ability
· At 3 months post-treatment, 17% of Cohort 1 and 67% of Cohort 2 patients met the statistical criteria for response for improved functional swallowing capacity (Cold-Water Timed Drinking Test)
· 100% of patients in Cohort 1 and Cohort 2 met the statistical criteria for response for improved total Sydney Swallow Questionnaire (SSQ) score at 3 months post-treatment
· 67% of patients in Cohort 1 and Cohort 2 met the statistical criteria for response for improved throat closing ability at 3 months post-treatment
· Pivotal study planned for mid-2027
Safety: There have been no Serious Adverse Events in any patient treated with BB-301 to date.
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