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Biofrontera Inc. Reports First Quarter 2026 Financial Results and Provides a Business Update

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Biofrontera (NASDAQ:BFRI) reported Q1 2026 revenue of $10.1 million, up ~17% from $8.6 million, driven by ~16% Ameluz unit growth and a price increase. Gross margin rose to about 80%, and operating loss was $4.3 million.

Net loss was $4.8 million ($0.41/share); Adjusted EBITDA improved to $(3.6) million. Cash stood at $6.3 million with minimal operating cash use. The company highlighted positive Phase 3 AK and Phase 2b acne data, FDA sNDA acceptance for sBCC with a September 28, 2026 PDUFA date, and regained Nasdaq bid-price compliance.

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Positive

  • Revenue grew ~17% year over year to $10.1 million
  • Gross margin expanded to about 80%, up 18 percentage points
  • Adjusted EBITDA loss improved by ~$0.8 million to $(3.6) million
  • Operating cash use only $70 thousand; cash balance $6.3 million
  • Approximately 16% growth in Ameluz units sold plus price increase
  • Positive Phase 3 AK and Phase 2b acne trial results reported
  • FDA accepted sNDA for sBCC with September 28, 2026 PDUFA date
  • Company regained compliance with Nasdaq minimum bid price requirement

Negative

  • Net loss widened to $4.8 million from $4.2 million
  • Operating loss remained high at $4.3 million in Q1 2026
  • Total operating expenses increased to $14.4 million from $13.1 million
  • SG&A rose to $11.0 million, including higher legal expenses
  • $1.2 million earnout expense recognized under new structure
  • Adjusted EBITDA margin still negative at (35.3)%

News Market Reaction – BFRI

+3.00% 1.9x vol
33 alerts
+3.00% Session close to close
+14.0% Peak Tracked
-36.1% Trough Tracked
$11.87M Market Cap
1.9x Rel. Volume

In the May 14 session, BFRI gained 3.00%, reflecting a moderate positive market reaction. Argus tracked a peak move of +14.0% during that session. Argus tracked a trough of -36.1% from its starting point during tracking. Our momentum scanner triggered 33 alerts that day, indicating elevated trading interest and price volatility. Trading volume was above average at 1.9x the daily average, suggesting increased trading activity.

Data tracked by StockTitan Argus on the day of publication.

Market Context

This announcement highlights Q1 2026 revenue of $10.1M, roughly 17% year-over-year growth, and gross...
Analysis

This announcement highlights Q1 2026 revenue of $10.1M, roughly 17% year-over-year growth, and gross margins near 80% following the Strategic Transaction with Biofrontera AG. Cash usage was minimal, with balance at $6.3M, while Adjusted EBITDA improved to -$3.6M. Clinically, positive Phase 3 AK and Phase 2b acne results, plus a September 2026 PDUFA date for sBCC, create multiple potential catalysts. Investors may track expense trends, net loss trajectory, and regulatory timelines to gauge sustainability of the improving profile.

Key Figures

Q1 2026 revenue: $10.1M Gross margin: ≈80% Operating loss: $4.3M +5 more
8 metrics
Q1 2026 revenue $10.1M Three months ended March 31, 2026; up from $8.6M in Q1 2025 (~17% growth)
Gross margin ≈80% Q1 2026 gross margin vs ≈62% in Q1 2025 after new earnout structure
Operating loss $4.3M Q1 2026 operating loss vs $4.5M in Q1 2025
Adjusted EBITDA -$3.6M Q1 2026 vs -$4.4M in Q1 2025; margin improved to (35.3)% from (51.0)%
Cash balance $6.3M Operating cash as of March 31, 2026 vs $1.8M in Q1 2025
Net loss per share $0.41 Q1 2026 net loss of $4.8M or $0.41 vs $4.2M or $0.47 in Q1 2025
SG&A expenses $11.0M Q1 2026 SG&A vs $8.7M in Q1 2025, driven by selling, legal, manufacturing costs
Acne lesion reduction 58% vs 37% Phase 2b AV trial; 3-hour Ameluz PDT vs vehicle PDT in inflammatory lesions

Previous Earnings Reports

5 past events · Latest: Mar 19 (Positive)
Same Type Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Mar 19 Q4/FY25 earnings Positive -1.5% Record Q4/FY25 revenue and margins plus strategic asset acquisition updates.
Nov 13 Q3 2025 earnings Negative -8.6% Q3 revenue decline, tight liquidity, and going concern commentary with restructuring.
Aug 13 Q2 2025 earnings Positive +1.7% Q2 revenue growth, new royalty structure, funding and IP gains for Ameluz.
May 15 Q1 2025 earnings Positive -7.2% Q1 revenue growth, pipeline progress, and improved net loss and EBITDA.
Mar 21 FY 2024 earnings Positive -16.5% Record FY24 revenue, cost reductions, improved cash, and clinical milestones.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Earnings releases have generally highlighted revenue growth and strategic progress, yet 3 of the last 5 similar announcements were followed by negative next-day moves, indicating a tendency for weak price responses to fundamentally positive updates.

Recent Company History

Over the past several earnings cycles, Biofrontera reported growing revenues and improving unit economics, including record FY 2024 revenue of $37.3M and Q4 2025 revenue of $17.1M with gross margin expansion. Strategic steps such as acquiring U.S. Ameluz and RhodoLED rights and shifting to a 12–15% royalty structure aimed to enhance profitability. Cash levels fluctuated but improved at key points. Today’s Q1 2026 update continues the theme of revenue growth, margin expansion, and cash preservation following the Strategic Transaction.

Key Terms

photodynamic therapy (pdt), actinic keratoses (aks), superficial basal cell carcinoma (sbcc), supplemental new drug application (snda), +4 more
8 terms
photodynamic therapy (pdt) medical
"a biopharmaceutical company specializing in the development and commercialization of photodynamic therapy (PDT) in dermatology"
Photodynamic therapy (PDT) is a medical treatment that uses special light-sensitive drugs and a light source to target and destroy abnormal or cancerous cells. It works like a precise spotlight, activating the drug only in the affected area to minimize damage to surrounding tissue. While primarily a health care method, its development and adoption can influence biotech and pharmaceutical markets, making it relevant for investors tracking advancements in medical technology.
actinic keratoses (aks) medical
"Phase 3 clinical trial evaluating Ameluz® PDT for the treatment of mild to moderate actinic keratoses (AKs) on the extremities"
Actinic keratoses (AKs) are small, rough patches or bumps on the skin caused by long-term sun exposure, often appearing on areas like the face, scalp, or hands. Though usually harmless, they can sometimes develop into skin cancer if left untreated. For investors, understanding AKs highlights the importance of health-related industries, such as skincare and medical treatments, which can be influenced by public health trends and aging populations.
superficial basal cell carcinoma (sbcc) medical
"Ameluz® PDT for the treatment of superficial basal cell carcinoma (sBCC), with a PDUFA target action date"
A superficial basal cell carcinoma (sBCC) is a common, slow-growing form of skin cancer that stays near the surface of the skin, often appearing as a scaly or reddish patch rather than a deep lump. Investors care because its high prevalence and tendency to be treated with topical drugs, minor procedures or recurring therapy creates steady demand, clinical trial opportunities and regulatory milestones that can materially affect companies focused on dermatology treatments.
supplemental new drug application (snda) regulatory
"completion of its filing review and filing acceptance of the Company's supplemental New Drug Application (sNDA) for Ameluz® PDT"
A supplemental new drug application (snda) is a formal request made to regulatory authorities to make changes to an already approved medication, such as adding new uses, adjusting dosages, or improving manufacturing processes. It’s similar to updating a product’s packaging or instructions after it has been approved for sale. For investors, an snda signals ongoing development or improvements that could impact a company’s future sales or regulatory approval prospects.
pdufa target action date regulatory
"with a PDUFA target action date of September 28, 2026"
The PDUFA target action date is the deadline set by the U.S. Food and Drug Administration (FDA) by which it aims to decide whether to approve or reject a new drug application. This date helps investors gauge when a company’s new medication might reach the market, potentially influencing sales and revenue expectations. It acts as a key milestone signaling progress in the drug approval process.
pharmacokinetics medical
"Announced database lock of Phase 1 pharmacokinetics study required for FDA filing"
Pharmacokinetics is the study of how a substance, such as a drug or chemical, moves through and is processed by the body over time. It tracks how it is absorbed, distributed, broken down, and eventually eliminated. For investors, understanding pharmacokinetics helps gauge the effectiveness, safety, and potential risks of new medications or treatments, which can influence a company’s success and valuation in the healthcare industry.
acne vulgaris (av) medical
"Phase 2b clinical trial for the treatment of moderate to severe acne vulgaris (AV)"
Acne vulgaris (AV) is a common skin condition that causes pimples, blackheads, whiteheads and sometimes deeper inflamed bumps when hair follicles become clogged and infected; think of it as tiny clogged drains on the skin that can swell and scar. For investors, AV matters because it creates steady demand for treatments across prescription drugs, over‑the‑counter products, medical devices and cosmetic procedures, so changes in clinical trial results, approvals, or insurance coverage can affect sales and company valuations.
adjusted ebitda financial
"Adjusted EBITDA for the first quarter of 2026 was $(3.6) million compared with $(4.4) million"
Adjusted EBITDA is a way companies measure how much money they make from their core operations, like running a business, by removing certain costs or income that aren’t part of regular business activities. It helps investors see how well a company is doing without distractions from unusual expenses or gains, making it easier to compare companies or track performance over time.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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Woburn, MA, May 14, 2026 (GLOBE NEWSWIRE) -- Biofrontera Inc. (NASDAQ: BFRI) (the "Company"), a biopharmaceutical company specializing in the development and commercialization of photodynamic therapy (PDT) in dermatology, today reported financial results for the three months ended March 31, 2026 and provided a business update.

First Quarter Financial Highlights

  • Revenues for Q1 2026 were $10.1 million, a ~17% increase compared to $8.6 million for the same period in 2025.
  • Gross margins were about 80%, an 18 percentage points increase compared to approximately 62% in Q1 2025, reflecting the first full quarter under the new earnout structure following the closing of the strategic transaction with Biofrontera AG in October 2025 (the “Strategic Transaction”).
  • Operating loss was $4.3 million in Q1 2026 compared to a loss of $4.5 million in Q1 2025.
  • Adjusted EBITDA improved to $(3.6) million from $(4.4) million in Q1 2025, an improvement of approximately $0.8 million reflecting expanded gross margins under the new earnout structure.
  • With $70 thousand used in operations, we largely maintained the operating cash balance we had at the end of Q4 2025, with $6.3 million as of March 31, 2026, compared to $1.8 million in Q1 2025.

Recent Operational Highlights

  • Announced FDA's completion of its filing review and filing acceptance of the Company's supplemental New Drug Application (sNDA) for Ameluz® PDT for the treatment of superficial basal cell carcinoma (sBCC), with a PDUFA target action date of September 28, 2026.
  • Announced positive and statistically significant top-line results from its Phase 3 clinical trial evaluating Ameluz® PDT for the treatment of mild to moderate actinic keratoses (AKs) on the extremities, neck, and trunk, meeting the primary endpoint.
  • Announced database lock of Phase 1 pharmacokinetics study required for FDA filing on treatment field on extremities, neck and trunk with a treatment area of up to 240 cm².
  • Announced positive results of its Phase 2b clinical trial for the treatment of moderate to severe acne vulgaris (AV), with a 58% reduction in inflammatory lesions in the 3-hour incubation protocol with Ameluz® PDT, compared to 37% with vehicle PDT (PPS).
  • Regained compliance with the Nasdaq Minimum Bid Price Requirement as confirmed by Nasdaq on May 6, 2026.

Hermann Luebbert, Chief Executive Officer and Chairman of Biofrontera Inc., stated: "The first quarter of 2026 marks the first full quarter under our new cost structure following the Strategic Transaction, and the results speak clearly. Revenue grew 17% year over year, gross margins expanded to approximately 80%, and our cash consumption was near zero—a dramatic improvement from $4.1 million of cash consumption in the prior-year quarter. Our results were further driven by continued commercial momentum leading to significant uptake of the Ameluz PDT platform by dermatologists and their patients.

At the same time, our clinical pipeline continues to advance at an accelerated pace. With a PDUFA date for sBCC in September 2026, positive Phase 3 results in AK on neck/trunk and extremities, and encouraging Phase 2b data in acne, we have multiple near-term catalysts that could meaningfully expand the commercial opportunity for the Ameluz platform.

We remain focused on our goal of reaching sustained profitability and cash-flow breakeven while setting the foundation for medium to long-term growth, and I believe we are well positioned to help our customers and their patients and build long-term value for our shareholders."

First Quarter Financial Results

Total revenues for the first quarter of 2026 were $10.1 million compared with $8.6 million for the first quarter of 2025. The 17% year-over-year growth was primarily driven by approximately 16% growth in the number of Ameluz units sold and a price increase implemented in the fourth quarter of 2025.

Gross profit margin in the first quarter of 2026 was approximately 80% compared to approximately 62% in Q1 2025. Cost of revenues, related party decreased by approximately 40% year over year, driven by the transition from the transfer pricing model under the prior license and supply agreement to the significantly lower earnout structure in place following the Strategic Transaction. The Company recognized $1.2 million in earnout expense during the quarter.

Total operating expenses were $14.4 million for the first quarter of 2026 compared with $13.1 million for the first quarter of 2025.

Selling, general and administrative expenses were $11.0 million for the first quarter of 2026 compared with $8.7 million for the first quarter of 2025. The increase was primarily driven by higher selling and marketing costs reflecting lower sales team turnover during the period leading to the full deployment of the direct sales team, increased legal expenses associated with ongoing patent-related claims, and manufacturing-related costs of $0.6 million assumed in connection with the Strategic Transaction.

Research and development expenses were $0.9 million for the first quarter of 2026 compared with $1.2 million for the first quarter of 2025. The decrease was primarily attributable to certain clinical trials reaching substantial completion.

The net loss for the first quarter of 2026 was $4.8 million, or $0.41 per share, compared with a net loss of $4.2 million, or $0.47 per share, for the prior-year quarter. The net loss comparison was impacted by a $0.8 million swing in the non-cash change in fair value of warrant liabilities.

Adjusted EBITDA for the first quarter of 2026 was $(3.6) million compared with $(4.4) million for the first quarter of 2025, an improvement of approximately $0.8 million. Adjusted EBITDA margin improved to (35.3)% from (51.0)% in the prior-year quarter. We look at Adjusted EBITDA, a non-GAAP financial measure, as an indication of ongoing operations, defined as net income or loss excluding interest income and expense, income taxes, depreciation and amortization, and certain other non-recurring or non-cash items.

Please refer to the table below which presents a GAAP to non-GAAP reconciliation of Adjusted EBITDA for the first quarters of 2026 and 2025.

Conference Call Details
Conference call: Thursday, May 14, 2026 at 11:00 AM ET

Conference Call:1-877-877-1275 (U.S./Canada)
1-412-858-5202 (international)
Webcast:Webcast – Biofrontera Inc. 1Q26 Results Conference Call
https://event.choruscall.com/mediaframe/webcast.html?webcastid=Re1hZKm0
  

About Biofrontera Inc.

Biofrontera Inc. is a U.S.-based biopharmaceutical company commercializing a portfolio of pharmaceutical products for the treatment of dermatological conditions with photodynamic therapy (PDT). The Company's products are used for the treatment of actinic keratoses, which are pre-cancerous skin lesions, and in development for additional indications. For more information, visit www.biofrontera-us.com and follow Biofrontera on LinkedIn and X.

Contacts Investor Relations
Ben Shamsian
Lytham Partners
646-829-9701
shamsian@lythampartners.com

Forward-Looking Statements

Certain statements in this press release may constitute "forward-looking statements" within the meaning of the United States Private Securities Litigation Reform Act of 1995. All statements, other than statements of historical facts, in this press release, including statements regarding our strategy, future operations, regulatory process, future financial position, future revenue, projected costs, prospects, plans, objectives of management and expected market growth, are forward-looking statements. The words "believe", "anticipate", "intend", "expect", "target", "goal", "estimate", "plan", "assume", "may", "will", "predict", "project", "would", "could" and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. You should read this press release and any documents referenced herein completely and with the understanding that our actual future results may be materially different from what we expect. While we have based these forward-looking statements on our current expectations and projections about future events, we may not actually achieve the plans, intentions or expectations disclosed in or implied by our forward-looking statements, and you should not place undue reliance on our forward-looking statements.

These forward-looking statements are subject to risks, uncertainties and assumptions about us and accordingly, actual results or events could differ materially from the plans, intentions and expectations disclosed in or implied by the forward-looking statements we make. These risks and uncertainties, many of which are beyond our control, include, but are not limited to: our ability to achieve and sustain profitability; our ability to compete effectively in selling our products; our ability to expand, manage and maintain our direct sales and marketing efforts, including our ability to obtain the financing to develop our marketing strategy, if needed; changes in our relationship with our manufacturing partners and the possible impact of tariffs; our ability to manufacture our products; our ability to adequately protect our intellectual property and operate the business without infringing upon the intellectual property rights of others; our actual financial results may vary significantly from forecasts and from period to period; our estimates regarding anticipated operating losses, future revenues, capital requirements and our needs for additional financing; market risks regarding consolidation and group purchasing organizations ("GPOs") in the healthcare industry; the willingness of healthcare providers to purchase our products if coverage, reimbursement and pricing from third-party payors for our products, or procedures using our products significantly declines; our ability to market, commercialize, achieve market acceptance for and sell our products; the fact that product quality issues or product defects may harm our business; any claims brought against the Company, including but not limited to product liability claims, claims of patent infringement, or claims challenging the validity of our intellectual property; our ability to maintain compliance with The Nasdaq Stock Market, LLC continued listing standards; our ability to comply with the requirements of being a public company; the progress, timing and completion of research, development and preclinical studies and clinical trials for our products; our ability to obtain and maintain the regulatory approvals necessary for the marketing of our products in the United States; and other factors that may be disclosed in the Company's filings with the Securities and Exchange Commission ("SEC"), which can be obtained on the SEC website at www.sec.gov. Our forward-looking statements do not reflect the potential impact of any future acquisitions, mergers, dispositions, joint ventures or investments that we may make. We do not assume any obligation to update any forward-looking statements, whether as a result of new information, future events or otherwise, except as required by law. Any forward-looking statements speak only as of the date on which they are made, and we undertake no obligation to publicly update or revise any forward-looking statements to reflect events or circumstances that may arise after the date of this press release, except as required by applicable law. Investors should evaluate any statements made by us in light of these important factors.

(Tables follow)

BIOFRONTERA INC.
CONDENSED CONSOLIDATED BALANCE SHEETS
(In thousands, except par value and share amounts)

  March 31, 2026
(Unaudited)
  December 31, 2025 
ASSETS      
Current assets:      
Cash and cash equivalents $6,317  $6,392 
Investment, related party  9   9 
Accounts receivable, net  3,879   7,291 
Inventories  1,231   1,426 
Prepaid expenses and other current assets  1,062   2,279 
Other assets, related party  661   686 
Total current assets  13,159   18,083 
         
Inventories, long term  3,591   3,729 
Property and equipment, net  2,175   2,158 
Operating lease right-of-use assets  2,895   1,584 
Intangible assets, net  2,609   2,650 
Other assets  358   360 
Total assets $24,787  $28,564 
         
LIABILITIES AND STOCKHOLDERS' EQUITY        
Current liabilities:        
Accounts payable $3,634  $1,855 
Accounts payable, related parties, net  1,315   4,811 
Operating lease liabilities  506   332 
Accrued expenses and other current liabilities  5,468   4,897 
Total current liabilities  10,923   11,895 
         
Long-term liabilities:        
Convertible notes payable, net  4,719   4,589 
Warrant liabilities  570   351 
Operating lease liabilities, non-current  2,499   1,240 
Other liabilities  6   9 
Total liabilities  18,717   18,084 
         
Total stockholders' equity  6,070   10,480 
Total liabilities and stockholders' equity $24,787  $28,564 


BIOFRONTERA INC.

CONSOLIDATED STATEMENTS OF OPERATIONS
(In thousands, except per share amounts and number of shares)

  Three Months Ended
March 31, 2026
(Unaudited)
  Three Months Ended
March 31, 2025
(Unaudited)
 
Product revenues, net $10,084  $8,588 
         
Operating expenses        
Cost of revenues, related party  1,831   3,075 
Cost of revenues, other  285   193 
Selling, general and administrative  10,994   8,653 
Selling, general and administrative, related party  2   7 
Patent remediation expense  392    
Research and development  900   1,207 
Total operating expenses  14,404   13,135 
         
Loss from operations  (4,320)  (4,547)
         
Other income (expense)        
Change in fair value of warrant liabilities  (219)  548 
Interest expense, net  (125)  (106)
Other expense, net  (88)  (99)
Total other income (expense)  (432)  343 
         
Loss before income taxes  (4,752)  (4,204)
Income tax benefit     (1)
Net loss $(4,752) $(4,203)
         
Loss per common share:        
Basic and diluted $(0.41) $(0.47)
         
Weighted-average common shares outstanding:        
Basic and diluted  11,683,323   8,873,932 


BIOFRONTERA INC.

CONSOLIDATED STATEMENTS OF CASH FLOWS
(In Thousands)

  Three Months Ended
March 31, 2026
(Unaudited)
  Three Months Ended
March 31, 2025
(Unaudited)
 
Cash flows from operating activities:      
Net loss $(4,752) $(4,203)
Adjustments to reconcile net loss to cash flows used in operations:        
Depreciation and amortization  55   29 
Reduction in the carrying amount of right-of-use assets  132   190 
Stock-based compensation  342   239 
Non-cash interest expense  130   119 
Allowance for credit losses  (1)  (46)
Change in fair value of warrant liabilities  219   (548)
Loss from termination of operating leases  1    
Changes in operating assets and liabilities:        
Accounts receivable  3,413   1,330 
Other receivables, related party  1   - 
Prepaid expenses and other assets  1,219   (224)
Other assets, related party  25    
Inventories  307   119 
Accounts payable  1,780   1,444 
Accounts payable, related parties, net  (3,497)  (2,694)
Operating lease liabilities  (10)  (179)
Accrued expenses and other liabilities  566   307 
Cash flows used in operating activities  (70)  (4,117)
         
Cash flows from investing activities        
Purchases of property and equipment  (5)  (3)
Cash flows used in investing activities  (5)  (3)
         
Net decrease in cash and cash equivalents  (75)  (4,120)
Cash, cash equivalents and restricted cash, at beginning of period  6,592   6,105 
Cash, cash equivalents and restricted cash, at end of period $6,517  $1,985 


BIOFRONTERA INC.

GAAP TO NON-GAAP ADJUSTED EBITDA RECONCILIATION
(In thousands)

  Three Months Ended
March 31, 2026
(Unaudited)
  Three Months Ended
March 31, 2025
(Unaudited)
 
Net loss $(4,752) $(4,203)
Interest expense, net  125   106 
Income tax expense     (1)
Depreciation and amortization  55   29 
EBITDA  (4,572)  (4,069)
         
Change in fair value of warrant liabilities  219   (548)
Stock-based compensation  342   239 
Patent remediation - inventory write-down  58    
Patent remediation expense  392    
Adjusted EBITDA $(3,561) $(4,378)
Adjusted EBITDA margin  (35.3)%  (51.0)%



FAQ

How did Biofrontera (NASDAQ:BFRI) perform financially in Q1 2026?

Biofrontera reported Q1 2026 revenue of $10.1 million, about 17% higher than $8.6 million in Q1 2025, according to Biofrontera. Net loss was $4.8 million, or $0.41 per share, and gross margin reached approximately 80%.

What drove Biofrontera’s revenue and margin growth in Q1 2026 (BFRI)?

Revenue growth was mainly driven by roughly 16% Ameluz unit growth and a price increase, according to Biofrontera. Gross margin rose to about 80%, helped by lower cost of revenues under the new earnout structure following the October 2025 strategic transaction.

What were Biofrontera’s Q1 2026 net loss and Adjusted EBITDA (BFRI)?

Biofrontera recorded a Q1 2026 net loss of $4.8 million, or $0.41 per share, according to Biofrontera. Adjusted EBITDA improved to $(3.6) million from $(4.4) million a year earlier, with Adjusted EBITDA margin improving to (35.3)%.

How strong was Biofrontera’s cash position at March 31, 2026 (BFRI)?

Biofrontera reported $6.3 million in cash as of March 31, 2026, according to Biofrontera. Operating activities used only $70 thousand during Q1 2026, indicating relatively stable operating cash compared with the end of Q4 2025 and $1.8 million in Q1 2025.

What clinical trial results did Biofrontera announce alongside Q1 2026 earnings?

Biofrontera announced positive, statistically significant top-line Phase 3 results for Ameluz PDT in actinic keratoses and positive Phase 2b acne data, according to Biofrontera. A Phase 1 pharmacokinetics study database was also locked, supporting future filings for larger treatment fields.

What is the status of Biofrontera’s sNDA for sBCC and its PDUFA date?

The FDA completed filing review and accepted Biofrontera’s sNDA for Ameluz PDT in superficial basal cell carcinoma, according to Biofrontera. The Prescription Drug User Fee Act (PDUFA) target action date is September 28, 2026, representing a key upcoming regulatory milestone.

Did Biofrontera (BFRI) regain Nasdaq listing compliance in 2026?

Yes, Biofrontera regained compliance with the Nasdaq Minimum Bid Price Requirement, as confirmed on May 6, 2026, according to Biofrontera. This confirmation indicates the company’s share price met Nasdaq’s minimum bid price criteria after previously being out of compliance.