Benitec Biopharma Releases Third Quarter 2026 Financial Results and Provides Operational Update
Rhea-AI Summary
Benitec Biopharma (NASDAQ:BNTC) reported Q3 2026 results and BB-301 updates. Total expenses were $13.6M vs. $15.3M a year ago, with net loss $11.9M ($0.24/share) vs. $14.5M. Cash was $184.8M, expected to fund BB-301 through its pivotal study.
BB-301 Phase 1b/2a data showed durable low-dose responses up to 24 months, deep disease-modifying efficacy at high dose, and no treatment-related severe adverse events. Cohort 2 enrollment is progressing, with updated interim data and an FDA pivotal-study design meeting expected in 2H 2026.
Positive
- Total quarterly expenses decreased to $13.6M from $15.3M year-over-year
- Net loss narrowed to $11.9M ($0.24/share) from $14.5M ($0.38/share)
- Cash and equivalents of $184.8M as of March 31, 2026
- Durable low-dose BB-301 responses at 12 and 24 months
- High-dose BB-301 shows deep, disease-modifying efficacy at 3 months
- No treatment-related severe adverse events reported in BB-301 study
Negative
- Quarterly net loss remains substantial at $11.9M
- Research and development expenses were $6.3M for the quarter
- General and administrative expenses were $7.3M for the quarter
News Market Reaction – BNTC
In the May 14 session, BNTC gained 1.72%, reflecting a mild positive market reaction.
Data tracked by StockTitan Argus on the day of publication.
Key Figures
Previous Earnings Reports
| Date | Event | Sentiment | 24h Move | Catalyst |
|---|---|---|---|---|
| Feb 12 | Q2 2026 earnings | Positive | -2.7% | Reported Q2 results with all Cohort 1 responders and strong cash balance. |
| Nov 14 | Q1 2026 earnings | Positive | +2.8% | Q1 2026 results, 100% responder rate, fast track, and major equity raise. |
| Sep 22 | FY 2025 results | Neutral | -2.1% | Full-year 2025 loss widened but cash remained strong and Cohort 2 advanced. |
| May 14 | Q3 2025 earnings | Neutral | +3.0% | Q3 2025 results with higher expenses, strong cash, and Cohort 1 completion. |
| Feb 14 | Q2 2025 earnings | Positive | +16.0% | Q2 2025 results with BB-301 interim efficacy and growing cash balance. |
24h Move is the share-price change in the day after each event; other market factors may also have contributed.
Earnings and financial updates have often triggered moderate moves in both directions, with a slight tilt toward positive reactions and one notably strong upside response.
Across the last five earnings/financial releases (from Feb 2025 through Feb 2026), Benitec consistently paired loss-making financials with advancing BB-301 clinical milestones and strengthening cash balances via equity financings. Price reactions ranged from modest declines to a strong double-digit gain, showing that investors respond to both dilution and clinical progress. Today’s Q3 2026 update continues the pattern of highlighting durable BB-301 efficacy, ongoing Cohort 2 enrollment, and a sizeable cash position to fund pivotal development.
Key Terms
phase 1b/2a medical
pivotal study medical
oculopharyngeal muscular dystrophy medical
dysphagia medical
gene therapy medical
dna-directed rna interference medical
warrants financial
AI-generated analysis. How Rhea-AI works. Not financial advice.
- Late-breaking abstract for BB-301 presented at the Muscular Dystrophy Association (MDA) Clinical and Scientific Conference in March demonstrated durable responses to low dose BB-301 at 12-months and 24-months post-treatment and further improvements in depth of response following treatment with high dose BB-301 at the 3-month post-treatment follow-up time-point, with both doses demonstrating disease modifying outcomes
- BB-301 Phase 1b/2a interim clinical study results selected for oral presentation at the 2026 American Society of Gene and Cell Therapy (ASGCT) Annual Meeting on May 15
- Advancement of Cohort 2 enrollment continues as Patient 1 and Patient 2 were both safely treated with high dose BB-301 in the ongoing Phase 1b/2a clinical study of BB-301; Benitec remains on track to provide updated interim clinical study results in 2H-2026
- The Company remains on track to engage with U.S. Food and Drug Administration (FDA) mid-year to formalize the BB-301 pivotal study design
- Benitec is well-capitalized to advance BB-301 through completion of the BB-301 pivotal study with cash as of March 31, 2026, of approximately
$184.8 million .
HAYWARD, Calif., May 14, 2026 (GLOBE NEWSWIRE) -- Benitec Biopharma Inc. (NASDAQ: BNTC) (“Benitec” or the “Company”), a clinical-stage, gene therapy-focused, biotechnology company developing novel genetic medicines based on its proprietary “Silence and Replace” DNA-directed RNA interference ("ddRNAi") platform, today announced financial results for its third fiscal quarter ended March 31, 2026, and provided a review of recent clinical study results and anticipated upcoming regulatory and clinical study milestones.
“This has been a critical period of continued advancements for the BB-301 clinical development program, marked by strongly encouraging clinical progress for patients treated with low dose BB-301 in Cohort 1 and the progression of enrollment for Cohort 2 with the safe treatment of Patient 1 and Patient 2 with high dose BB-301,” said Jerel A. Banks, M.D., Ph.D., Executive Chairman and Chief Executive Officer of Benitec. “We look forward to the meaningful milestones ahead, including expanding visibility of our interim clinical study results and engaging with the FDA to confirm the pivotal study design required to support BB-301 approval. We are well-positioned to continue to advance BB-301, the first and only potential disease-modifying therapy for the treatment of Oculopharyngeal Muscular Dystrophy (OPMD)-related dysphagia and are now one step closer to reaching the patients and families of the OPMD community.”
Recent Clinical Study Highlights
The Company continues to advance the BB-301 Phase 1b/2a Clinical Study evaluating the safety and clinical efficacy of locally-delivered BB-301 for the treatment of OPMD-related dysphagia.
- Key interim clinical study results were presented at the 2026 MDA Clinical & Scientific Conference demonstrating durable responses to low dose BB-301 at 12-months and 24-months and further improvements in depth of response following treatment with high dose BB-301 at the 3-month post-treatment follow-up time-point.
- BB-301 Phase 1b/2a interim clinical study results have been selected for oral presentation at the 2026 ASGCT Annual Meeting on May 15 in Boston, MA.
BB-301 Development Program Updates
All six Cohort 1 patients have safely completed the 12-month post-BB-301-treatment follow-up period and continue to experience robust responses to the low dose of BB-301.
The first two Cohort 2 patients have been safely treated with the high dose of BB-301, and available interim clinical results continue to demonstrate deep, disease-modifying efficacy for the high dose of BB-301.
No treatment-related severe adverse events have been observed.
Upcoming Regulatory and Clinical Milestones
- The Company remains on track to engage with FDA mid-year to formalize the BB-301 pivotal study design.
- Benitec remains on track to provide updated interim clinical study results for Cohort 1 patients and Cohort 2 patients in 2H-2026.
Financial Highlights
Third Quarter 2026 Financial Results
Total Expenses for the quarter ended March 31, 2026, were
The loss from operations for the quarter ended March 31, 2026, was
About BB-301
BB-301 is a novel, modified AAV9 capsid expressing a unique, single bifunctional construct promoting co-expression of both codon-optimized Poly-A Binding Protein Nuclear-1 (PABPN1) and two small inhibitory RNAs (siRNAs) against mutant PABPN1 (the causative gene for OPMD). The two siRNAs are modeled into microRNA backbones to silence expression of faulty mutant PABPN1, while allowing expression of the codon-optimized PABPN1 to replace the mutant with a functional version of the protein. We believe the silence and replace mechanism of BB-301 is uniquely positioned for the treatment of OPMD by halting mutant PABPN1 expression while providing a functional replacement protein. BB-301 has received Orphan Drug Designation from the EMA and Orphan Drug and Fast Track Designations from the FDA.
About Benitec Biopharma, Inc.
Benitec Biopharma Inc. (“Benitec” or the “Company”) is a clinical-stage biotechnology company focused on the advancement of novel genetic medicines with headquarters in Hayward, California. The proprietary “Silence and Replace” DNA-directed RNA interference platform combines RNA interference, or RNAi, with gene therapy to create medicines that simultaneously facilitate sustained silencing of disease-causing genes and concomitant delivery of wildtype replacement genes following a single administration of the therapeutic construct. The Company is developing Silence and Replace-based therapeutics for chronic and life-threatening human conditions including Oculopharyngeal Muscular Dystrophy (OPMD). A comprehensive overview of the Company can be found on Benitec’s website at www.benitec.com.
Forward Looking Statements
Except for the historical information set forth herein, the matters set forth in this press release include forward-looking statements, including statements regarding Benitec’s plans to develop and commercialize its product candidates, the timing of the completion of preclinical and clinical trials, the timing of the availability of data from our clinical trials, the timing and sufficiency of patient enrollment and dosing in clinical trials, the timing of expected regulatory filings and other regulatory steps, and the clinical utility and potential attributes and benefits of ddRNAi and Benitec’s product candidates, and other forward looking statements.
These forward-looking statements are based on the Company’s current expectations and subject to risks and uncertainties that may cause actual results to differ materially, including unanticipated developments in and risks related to: the success of our plans to develop and potentially commercialize our product candidates; the timing of the completion of preclinical studies and clinical trials; the timing and sufficiency of patient enrollment and dosing in any future clinical trials; the timing of the availability of data from our clinical trials; the timing and outcome of regulatory filings and approvals; the development of novel AAV vectors; our potential future out-licenses and collaborations; the plans of licensees of our technology; the clinical utility and potential attributes and benefits of ddRNAi and our product candidates, including the potential duration of treatment effects and the potential for a “one shot” cure; our intellectual property position and the duration of our patent portfolio; expenses, ongoing losses, future revenue, capital needs and needs for additional financing, and our ability to access additional financing given market conditions and other factors; the length of time over which we expect our cash and cash equivalents to be sufficient to execute on our business plan; unanticipated delays; further research and development and the results of clinical trials possibly being unsuccessful or insufficient to meet applicable regulatory standards or warrant continued development; the ability to enroll sufficient numbers of subjects in clinical trials; determinations made by the FDA and other governmental authorities and other regulatory developments; the Company’s ability to protect and enforce its patents and other intellectual property rights; the Company’s dependence on its relationships with its collaboration partners and other third parties; the efficacy or safety of the Company’s products and the products of the Company’s collaboration partners; the acceptance of the Company’s products and the products of the Company’s collaboration partners in the marketplace; market competition; sales, marketing, manufacturing and distribution requirements; greater than expected expenses; expenses relating to litigation or strategic activities; the impact of, and our ability to remediate, the identified material weakness in our internal control over financial reporting; the Company’s ability to satisfy its capital needs through increasing revenue and obtaining additional financing; the impact of local, regional, and national and international economic conditions and events; and other risks detailed from time to time in the Company’s reports filed with the Securities and Exchange Commission. The Company disclaims any intent or obligation to update these forward-looking statements.
Investor Relations Contact:
Candice Masse
astr partners
candice.masse@astrpartners.com
Media Contact:
Audra Friis
Sam Brown Healthcare Communications
(917) 519-9577
audrafriis@sambrown.com
Source: Benitec Biopharma Inc.
| BENITEC BIOPHARMA INC. Consolidated Balance Sheets (in thousands, except par value and share amounts) | ||||||||
| March 31, 2026 | June 30, 2025 | |||||||
| (Unaudited) | ||||||||
| Assets | ||||||||
| Current assets: | ||||||||
| Cash and cash equivalents | $ | 184,761 | $ | 97,744 | ||||
| Restricted cash | 114 | 113 | ||||||
| Trade and other receivables | 3 | 33 | ||||||
| Prepaid and other assets | 1,139 | 628 | ||||||
| Total current assets | 186,017 | 98,518 | ||||||
| Property and equipment, net | 116 | 131 | ||||||
| Deposits | 55 | 55 | ||||||
| Prepaid and other assets | 12 | 28 | ||||||
| Right-of-use assets | 800 | 860 | ||||||
| Total assets | $ | 187,000 | $ | 99,592 | ||||
| Liabilities and stockholders’ equity | ||||||||
| Current liabilities: | ||||||||
| Trade and other payables | $ | 2,251 | $ | 1,022 | ||||
| Accrued employee benefits | 541 | 426 | ||||||
| Lease liabilities, current portion | 482 | 354 | ||||||
| Total current liabilities | 3,274 | 1,802 | ||||||
| Lease liabilities, less current portion | 394 | 495 | ||||||
| Total liabilities | 3,668 | 2,297 | ||||||
| Stockholders’ equity: | ||||||||
| Preferred stock, | — | — | ||||||
| Common stock, | 3 | 2 | ||||||
| Additional paid-in capital | 445,194 | 326,308 | ||||||
| Accumulated deficit | (260,913 | ) | (228,176 | ) | ||||
| Accumulated other comprehensive loss | (952 | ) | (839 | ) | ||||
| Total stockholders’ equity | 183,332 | 97,295 | ||||||
| Total liabilities and stockholders’ equity | $ | 187,000 | $ | 99,592 | ||||
| BENITEC BIOPHARMA INC. Consolidated Statements of Operations and Comprehensive Loss (Unaudited) (in thousands, except share and per share amounts) | ||||||||||||||||
| Three Months Ended | Nine Months Ended | |||||||||||||||
| March 31, | March 31, | |||||||||||||||
| 2026 | 2025 | 2026 | 2025 | |||||||||||||
| Revenue: | ||||||||||||||||
| $ | — | $ | — | $ | — | $ | — | |||||||||
| Total revenues | — | — | — | — | ||||||||||||
| Operating expenses | ||||||||||||||||
| Research and development | 6,298 | 6,495 | 15,502 | 15,465 | ||||||||||||
| General and administrative | 7,284 | 8,840 | 21,260 | 16,466 | ||||||||||||
| Total operating expenses | 13,582 | 15,335 | 36,762 | 31,931 | ||||||||||||
| Loss from operations | (13,582 | ) | (15,335 | ) | (36,762 | ) | (31,931 | ) | ||||||||
| Other income (loss): | ||||||||||||||||
| Foreign currency transaction gain (loss) | 70 | 11 | 112 | (190 | ) | |||||||||||
| Interest income, net | 1,594 | 823 | 3,995 | 2,250 | ||||||||||||
| Other expense, net | (17 | ) | — | (82 | ) | (5 | ) | |||||||||
| Gain on extinguishment of liabilities | — | — | — | 764 | ||||||||||||
| Total other income, net | 1,647 | 834 | 4,025 | 2,819 | ||||||||||||
| Net loss | $ | (11,935 | ) | $ | (14,501 | ) | $ | (32,737 | ) | $ | (29,112 | ) | ||||
| Other comprehensive income: | ||||||||||||||||
| Unrealized foreign currency translation gain (loss) | (69 | ) | (28 | ) | (113 | ) | 176 | |||||||||
| Total other comprehensive income (loss) | (69 | ) | (28 | ) | (113 | ) | 176 | |||||||||
| Total comprehensive loss | $ | (12,004 | ) | $ | (14,529 | ) | $ | (32,850 | ) | $ | (28,936 | ) | ||||
| Net loss | $ | (11,935 | ) | $ | (14,501 | ) | $ | (32,737 | ) | $ | (29,112 | ) | ||||
| Net loss attributable to common shareholders | $ | (11,935 | ) | $ | (14,501 | ) | $ | (32,737 | ) | $ | (29,112 | ) | ||||
| Net loss per share: | ||||||||||||||||
| Basic and diluted | $ | (0.24 | ) | $ | (0.38 | ) | $ | (0.72 | ) | $ | (0.84 | ) | ||||
| Weighted average number of shares outstanding: basic and diluted | 49,386,203 | 38,599,453 | 45,598,553 | 34,559,870 | ||||||||||||
