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ADC Therapeutics Reports First Quarter 2026 Financial Results and Provides Operational Updates

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ADC Therapeutics (NYSE: ADCT) reported Q1 2026 results and provided clinical updates. Q1 net product revenue was $20.0M; net loss was $33.0M ($0.21/share) and adjusted net loss was $19.7M ($0.13/share). Cash and cash equivalents totaled $231.0M with a runway at least into 2028. Key clinical catalysts: LOTIS-5 topline expected in 2Q 2026 and full LOTIS-5 and LOTIS-7 data anticipated by year-end.

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Positive

  • Product revenues of $20.0M in Q1 2026 (up from $17.4M)
  • Cash and cash equivalents of $231.0M with runway into 2028
  • LOTIS-5 topline results expected in 2Q 2026 (near-term catalyst)
  • R&D expense decreased to $19.9M from $28.9M year-over-year
  • Total adjusted operating expenses reduced to $42.9M from $49.1M

Negative

  • Net loss of $33.0M (Q1 2026), or $0.21 per share
  • Cash balance declined from $261.3M at year-end to $231.0M
  • Selling and marketing expense rose to $12.7M from $10.6M

News Market Reaction – ADCT

-3.92%
6 alerts
-3.92% Session close to close
-18.7% Trough in 2 hr 26 min
$489.04M Market Cap
0.1x Rel. Volume

In the May 4 session, ADCT declined 3.92%, reflecting a moderate negative market reaction. Argus tracked a trough of -18.7% from its starting point during tracking. Our momentum scanner triggered 6 alerts that day, indicating moderate trading interest and price volatility.

Data tracked by StockTitan Argus on the day of publication.

Market Context

This announcement delivered Q1 2026 results showing higher ZYNLONTA product revenues, reduced operat...
Analysis

This announcement delivered Q1 2026 results showing higher ZYNLONTA product revenues, reduced operating expenses and a net loss improvement, alongside cash and equivalents of $231.0 million and an expected runway at least into 2028. It reiterated key clinical milestones, including LOTIS-5 Phase 3 topline data in 2Q 2026 and LOTIS-7 data by year-end. Investors may watch future earnings for revenue trajectory, LOTIS readouts, and any use of warrant-related resale capacity.

Key Figures

Net product revenue: $20.0 million License revenue & royalties: $0.8 million R&D expense: $19.9 million +5 more
8 metrics
Net product revenue $20.0 million First quarter 2026; vs $17.4 million in Q1 2025
License revenue & royalties $0.8 million First quarter 2026; vs $5.6 million in Q1 2025
R&D expense $19.9 million First quarter 2026; vs $28.9 million in Q1 2025
Total operating expenses $46.1 million First quarter 2026; vs $51.5 million in Q1 2025
Net loss $33.0 million ($0.21/share) First quarter 2026; vs $38.6 million ($0.36/share) in Q1 2025
Adjusted net loss $19.7 million ($0.13/share) First quarter 2026; vs $24.0 million ($0.22/share) in Q1 2025
Cash & cash equivalents $231.0 million As of March 31, 2026; down from $261.3 million on Dec 31, 2025
Cash runway At least into 2028 Company expectation based on March 31, 2026 cash position

Previous Earnings Reports

5 past events · Latest: Mar 10 (Positive)
Same Type Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Mar 10 Q4/FY 2025 earnings Positive +13.5% Fourth quarter and full-year 2025 results plus cash and LOTIS-5/7 updates.
Nov 10 Q3 2025 earnings Positive +4.2% Q3 2025 results, PIPE financing, and strong LOTIS-7 follicular lymphoma data.
Nov 10 Q3 2025 earnings Positive +4.2% Repeated Q3 2025 update with revenue, net loss, and pipeline progress.
Aug 12 Q2 2025 earnings Positive +9.7% Q2 2025 results, $100M PIPE, restructuring, and strong LOTIS-7 efficacy data.
May 14 Q1 2025 earnings Positive +37.1% Q1 2025 results with promising LOTIS-7 data and ZYNLONTA revenue growth.

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

Pattern Detected

Earnings/operational updates that pair financial results with ZYNLONTA clinical progress have historically led to positive share reactions, with all recent earnings-tagged events showing gains.

Recent Company History

Over the past year, ADC Therapeutics’ earnings releases have consistently combined ZYNLONTA clinical updates with funding and runway disclosures. Events on May 14, 2025, Aug 12, 2025, Nov 10, 2025, and Mar 10, 2026 all reported growing product revenues, sizable net losses, and extended cash runway into at least 2028, often supported by PIPE financings or royalty deals. These updates also highlighted LOTIS-5 and LOTIS-7 progress, similar to today’s emphasis on upcoming LOTIS readouts and a multiyear cash runway.

Key Terms

Phase 3, topline results, supplemental Biologics License Application, U.S. Food and Drug Administration, +3 more
7 terms
Phase 3 medical
"LOTIS-5 Phase 3 confirmatory trial of ZYNLONTA..."
Phase 3 is the late-stage clinical testing step for a new drug or medical treatment, where the product is given to large groups of patients to confirm effectiveness, monitor side effects, and compare it to standard care. Successful Phase 3 results are often the final scientific hurdle before regulators decide on approval and market launch—like passing a final exam before graduation—and can sharply change a company's valuation and future revenue prospects.
topline results medical
"LOTIS-5 topline results anticipated in 2Q 2026..."
Topline results are the initial, high-level summary of the most important outcomes from an event such as a clinical trial or a company reporting period — for a drug study this means whether the main goals were met and basic safety info, and for a company it often means headline revenue and profit figures. Investors care because these summaries act like a headline that quickly signals whether prospects have improved or worsened, often driving immediate market reactions before the full details are released.
supplemental Biologics License Application regulatory
"the Company intends to submit a supplemental Biologics License Application (sBLA)..."
A supplemental biologics license application is a formal request to a regulator (such as the U.S. Food and Drug Administration) asking permission to change an already approved biological product — for example to add a new use, change how it’s made, or alter dosing. For investors, an approved supplemental application can expand a product’s sales or reduce manufacturing risk, while a delay or rejection can limit revenue prospects or raise compliance costs; think of it like applying for an update to a building permit for an existing, income-producing property.
U.S. Food and Drug Administration regulatory
"submit a supplemental Biologics License Application (sBLA) to the U.S. Food and Drug Administration (FDA)..."
The U.S. Food and Drug Administration is the federal agency that evaluates and enforces safety, effectiveness and labeling standards for medicines, medical devices, vaccines, food and related products before they reach consumers. For investors it matters because FDA approvals, warnings or recalls determine whether a product can be sold, how quickly it reaches the market and how costly compliance will be—changes that directly affect a company’s revenue, costs and stock value.
diffuse large B-cell lymphoma medical
"confirmatory approval in 2L+ diffuse large B-cell lymphoma (DLBCL) thereafter."
A fast-growing form of blood cancer that starts in white blood cells within the lymphatic system and can spread quickly to other organs. Investors watch it because the need for effective treatments, the size of the patient population, and results from clinical trials or regulatory approvals can significantly affect pharmaceutical and biotech company revenues—think of it like a large, urgent market for new medicines where trial results or approvals can move stock prices.
DLBCL medical
"patients with relapsed or refractory (r/r) DLBCL is ongoing..."
Diffuse large B-cell lymphoma (DLBCL) is an aggressive type of blood cancer that starts in B cells, the immune system’s antibody-producing cells, and often grows quickly in lymph nodes or other organs. For investors, DLBCL matters because its severity drives demand for effective diagnostics and treatments, influencing drug development, clinical trial activity, regulatory decisions, and potential healthcare costs—similar to how a fast-moving fire spurs urgent demand for better firefighting tools.
bispecific antibody medical
"LOTIS-7 Phase 1b trial evaluating ZYNLONTA in combination with the bispecific antibody glofitamab..."
A bispecific antibody is a specially designed protein that can attach to two different targets at the same time. Think of it as a custom-made connector that brings two things together—such as a disease cell and an immune system component—helping the body fight illnesses more effectively. For investors, understanding bispecific antibodies is important because they represent innovative therapies that could lead to new treatments and potentially lucrative market opportunities.

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

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LOTIS-5 Phase 3 topline data expected in second quarter 2026, with full data for LOTIS-5 and LOTIS-7 anticipated by year end

First quarter 2026 net product revenue of $20.0 million

Cash and cash equivalents of $231.0 million as of March 31, 2026, with an expected cash runway at least into 2028

Company to host conference call today at 8:30 a.m. EDT

LAUSANNE, Switzerland, May 4, 2026 /PRNewswire/ -- ADC Therapeutics SA (NYSE: ADCT), a commercial-stage global leader and pioneer in the field of antibody drug conjugates (ADCs), today reported financial results for the first quarter ended March 31, 2026, and provided recent operational updates.

"During the first quarter, we continued to build momentum across our ZYNLONTA program," said Ameet Mallik, Chief Executive Officer of ADC Therapeutics. "Looking ahead, we have multiple near-term catalysts, including topline results from LOTIS-5 anticipated in the second quarter, full results expected from both LOTIS-5 and LOTIS-7 by year-end, as well as additional updates from the investigator-initiated studies in indolent lymphomas ahead. We believe that we are well-positioned to expand ZYNLONTA's role across B-cell malignancies, accelerating our expected growth trajectory starting in 2027."

First Quarter 2026 Operational Updates and Upcoming Milestones

LOTIS-5 topline results anticipated in 2Q 2026. The Company continues to expect to announce topline results from the LOTIS-5 Phase 3 confirmatory trial of ZYNLONTA® (loncastuximab tesirine-lpyl) in combination with rituximab in the second quarter of 2026, with full results anticipated by year-end. If positive, the Company intends to submit a supplemental Biologics License Application (sBLA) to the U.S. Food and Drug Administration (FDA) before year-end, with potential compendia inclusion in the first half of 2027 and confirmatory approval in 2L+ diffuse large B-cell lymphoma (DLBCL) thereafter.

LOTIS-7 trial ongoing with data anticipated by year-end. The LOTIS-7 Phase 1b trial evaluating ZYNLONTA in combination with the bispecific antibody glofitamab (COLUMVI®) in patients with relapsed or refractory (r/r) DLBCL is ongoing, with expected completion of enrollment at the selected 150 µg/kg dose in the first half of 2026. The Company plans to share full data at a medical meeting and through publication by the end of 2026. The Company also intends to evaluate potential regulatory and compendia pathways.

Investigator-Initiated trials (IITs) evaluating ZYNLONTA in additional B-cell malignancies progressing. The University of Miami Sylvester Comprehensive Cancer Center-led multi-center trials of ZYNLONTA in combination with rituximab to treat r/r follicular lymphoma (FL) and ZYNLONTA as a monotherapy to treat marginal zone lymphoma (MZL) are ongoing. The Company anticipates publication of data from both IITs between the end of 2026 and mid-2027. Assuming positive data, the Company intends to assess potential regulatory and compendia pathways.

First Quarter 2026 Financial Results

Product Revenues: Net product revenues were $20.0 million for the first quarter of 2026, as compared to $17.4 million for the first quarter of 2025. The increase in revenue versus the prior year was primarily driven by volume increase, which reflects the normal variability in customer ordering patterns as well as higher price.

License Revenues and Royalties: License revenue and royalties were $0.8 million for the first quarter of 2026, as compared to $5.6 million for the first quarter of 2025. The decrease was primarily driven by a prior year milestone received from our partner.

Cost of Product Sales: Cost of product sales was $3.6 million for the first quarter of 2026, as compared to $2.1 million for the first quarter of 2025. The increase in cost of product sales was primarily attributable to a $1.2 million increase in certain personnel costs, which includes a change in focus of these personnel from research and development clinical supply activities to commercial manufacturing activities.

Research and Development (R&D) Expense: R&D expense was $19.9 million for the first quarter of 2026, as compared to $28.9 million for the first quarter of 2025. The decrease was primarily driven by a $6.1 million decrease in external costs as a result of discontinued programs and completion of the IND-enabling activities for our PSMA-targeting ADC. The decrease was also driven by a shift of certain personnel costs totaling $2.1 million to cost of product sales ($1.2 million), inventory capitalization ($0.6 million), and selling and marketing expense ($0.3 million), reflecting a change in focus of these personnel from research and development activities toward commercial manufacturing and fulfillment activities.

Selling and Marketing (S&M) Expense: S&M expense was $12.7 million for the first quarter of 2026, as compared to $10.6 million for the first quarter of 2025. The increase was primarily due to higher wages and benefits, and marketing and advertising expenses.

General & Administrative (G&A) Expense: G&A expense was $9.9 million for the first quarter of 2026, as compared to $10.0 million for the first quarter of 2025.

Total Operating Expenses and Adjusted Total Operating Expenses: Total operating expenses were $46.1 million for the first quarter of 2026, as compared to $51.5 million for the first quarter of 2025. On a non-GAAP basis, total adjusted operating expenses were $42.9 million for the first quarter of 2026, as compared to $49.1 million for the first quarter of 2025. The reduction in total adjusted operating expenses was primarily driven by lower R&D expenses.

Net Loss and Adjusted Net Loss: Net loss for the first quarter of 2026 was $33.0 million, or a net loss of $0.21 per basic and diluted share, as compared to a net loss of $38.6 million, or a net loss of $0.36 per basic and diluted share, for the first quarter of 2025. Adjusted net loss, which is a non-GAAP financial measure, was $19.7 million, or an adjusted net loss of $0.13 per basic and diluted share, for the first quarter of 2026, as compared to adjusted net loss of $24.0 million, or $0.22 per basic and diluted share, for the first quarter of 2025. The lower net loss and adjusted net loss were primarily due to lower operating expenses and on a per basic and diluted share basis, by a higher number of weighted average shares outstanding.

Cash and Cash Equivalents: As of March 31, 2026, cash and cash equivalents were $231.0 million, compared to $261.3 million as of December 31, 2025, a change primarily driven by cash used in operations and for annual bonus payments. The Company has an expected cash runway at least into 2028.

Conference Call Details

ADC Therapeutics management will host a conference call and live audio webcast to discuss first quarter 2026 financial results and provide a company update today at 8:30 a.m. EDT. To access the conference call, please register here. Registrants will receive the dial-in number and unique PIN. It is recommended that you join 10 minutes before the event, though you may pre-register at any time. A live webcast of the call will be available under "Events & Presentations" in the Investors section of the ADC Therapeutics website at ir.adctherapeutics.com. The archived webcast will be available for 30 days following the call.

About ADC Therapeutics

ADC Therapeutics (NYSE: ADCT) is a commercial-stage global leader and pioneer in the field of antibody drug conjugates (ADCs), transforming treatment for patients through our focused portfolio with ZYNLONTA (loncastuximab tesirine-lpyl).

ADC Therapeutics' CD19-directed ADC ZYNLONTA received accelerated approval by the FDA and conditional approval from the European Commission for the treatment of relapsed or refractory diffuse large B-cell lymphoma after two or more lines of systemic therapy. ZYNLONTA is also in development in combination with other agents and in earlier lines of therapy.

Headquartered in Lausanne (Biopôle), Switzerland, with operations in New Jersey, ADC Therapeutics is focused on driving innovation in ADC development with specialized capabilities from clinical to manufacturing and commercialization. Learn more at https://adctherapeutics.com/ and follow us on LinkedIn.

Use of Non-GAAP Financial Measures

In addition to financial information prepared in accordance with U.S. Generally Accepted Accounting Principles (GAAP), this document also contains certain non-GAAP financial measures based on management's view of performance including:

  • Adjusted total operating expenses
  • Adjusted net loss
  • Adjusted net loss per share

Management uses such measures internally when monitoring and evaluating our operational performance, generating future operating plans and making strategic decisions regarding the allocation of capital. We believe that these adjusted financial measures provide useful information to investors and others in understanding and evaluating our operating results in the same manner as our management and facilitate operating performance comparability across both past and future reporting periods. These non-GAAP measures have limitations as financial measures and should be considered in addition to, and not in isolation or as a substitute for, the information prepared in accordance with GAAP. When preparing these supplemental non-GAAP measures, management typically excludes certain GAAP items that management does not believe are indicative of our ongoing operating performance. Furthermore, management does not consider these GAAP items to be normal, recurring cash operating expenses; however, these items may not meet the GAAP definition of unusual or non-recurring items. Since non-GAAP financial measures do not have standardized definitions and meanings, they may differ from the non-GAAP financial measures used by other companies, which reduces their usefulness as comparative financial measures. Because of these limitations, you should consider these adjusted financial measures alongside other GAAP financial measures.

The following items are excluded from adjusted total operating expenses:

Shared-Based Compensation Expense: We exclude share-based compensation expense from our adjusted financial measures because share-based compensation expense, which is non-cash, fluctuates from period to period based on factors that are not within our control, such as our stock price on the dates share-based grants are issued. Share-based compensation expense has been, and will continue to be for the foreseeable future, a recurring expense in our business and an important part of our compensation strategy.

Restructuring, Impairment and Other Related Costs: We exclude from our adjusted financial measures costs associated with our execution of certain strategies and initiatives to streamline operations, achieve targeted cost reductions or reprioritize research and development activities. These costs may include employee severance, contract termination costs, facility closing and exit costs, asset impairment charges (which are non-cash) and other costs that we believe do not represent the performance of our business or have a direct correlation to our ongoing or future business operations.

The following items are excluded from adjusted net loss and adjusted net loss per share:

Shared-Based Compensation Expense: We exclude share-based compensation expense from our adjusted financial measures because share-based compensation expense, which is non-cash, fluctuates from period to period based on factors that are not within our control, such as our stock price on the dates share-based grants are issued. Share-based compensation expense has been, and will continue to be for the foreseeable future, a recurring expense in our business and an important part of our compensation strategy.

Certain Other Items: We exclude certain other significant items that we believe do not represent the performance of our business, from our adjusted financial measures. Such items are evaluated by management on an individual basis based on both quantitative and qualitative aspects of their nature. While not all-inclusive, examples of certain other significant items excluded from our adjusted financial measures would be: restructuring, impairment and other related costs, changes in the fair value of warrant obligations and the effective interest expense associated with the senior secured term loan facility and the effective interest expense and cumulative catch-up adjustments associated with the deferred royalty obligation under the royalty purchase agreement with HealthCare Royalty Partners.

See the attached Reconciliation of GAAP Measures to Non-GAAP Measures for explanations of the amounts excluded and included to arrive at the non-GAAP financial measures.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. In some cases you can identify forward-looking statements by terminology such as "may", "will", "should", "would", "expect", "intend", "plan", "anticipate", "believe", "estimate", "predict", "potential", "seem", "seek", "future", "continue", or "appear" or the negative of these terms or similar expressions, although not all forward-looking statements contain these identifying words. Forward-looking statements are subject to certain risks and uncertainties that can cause actual results to differ materially from those described. Factors that may cause such differences include, but are not limited to: the timing of the  topline data release for LOTIS-5 and the results of the trial, the timing for the sBLA submission, acceptance and outcome of review of the sBLA submission, and full FDA approval; the Company's ability to grow ZYNLONTA® revenue in the United States and potential peak revenue; whether future LOTIS-7 clinical trial results will be consistent with or different from the LOTIS-7 data presented by the Company on December 3, 2025, the timing, publication and outcome of the full LOTIS-7 trial, compendia inclusion and regulatory strategy and the commercial opportunity; expected cash runway at least into 2028 which assumes use of minimum liquidity amount required to be maintained under its loan agreement covenants; the ability of our partners to commercialize ZYNLONTA® in foreign markets, the timing and amount of future revenue and payments to us from such partnerships and their ability to obtain regulatory approval for ZYNLONTA® in foreign jurisdictions; the timing and results of the Company's clinical trials; the timing, publication and results of investigator-initiated trials including those studying FL and MZL and the potential regulatory and/or compendia strategy and the future opportunity; the timing and outcome of regulatory submissions for the Company's products or product candidates; actions by the FDA or foreign regulatory authorities; projected revenue and expenses; the Company's indebtedness, including HealthCare Royalty Management and Blue Owl and Oaktree facilities, and the restrictions imposed on the Company's activities by such indebtedness, the ability to comply with the terms of the various agreements and repay such indebtedness, the impact on our future revenue streams, and the significant cash required to service such indebtedness; the Company's ability to obtain financial and other resources for its research, development, clinical, and commercial activities; and the uncertainties of international trade policies, including tariffs, sanctions, trade barriers and most favored nation drug pricing and the potential impact they may have on our business, financial condition, and results of operations. Additional information concerning these and other factors that may cause actual results to differ materially from those anticipated in the forward-looking statements is contained in the "Risk Factors" section of the Company's Annual Report on Form 10-K and in the Company's other periodic and current reports and filings with the U.S. Securities and Exchange Commission. These statements involve known and unknown risks, uncertainties and other factors that may cause actual results, performance, achievements or prospects to be materially different from any future results, performance, achievements or prospects expressed in or implied by such forward-looking statements. The Company cautions investors not to place undue reliance on the forward-looking statements contained in this document.

ADC Therapeutics SA

Condensed Consolidated Statements of Operations (Unaudited)

(in thousands, except for share and per share data)




Three Months Ended March 31,



2026


2025

Revenue





Product revenues, net


$        20,033


$       17,404

License revenues and royalties


818


5,629

Total revenue, net


20,851


23,033

Operating expense





Cost of product sales


(3,615)


(2,061)

Research and development


(19,877)


(28,928)

Selling and marketing


(12,708)


(10,553)

General and administrative


(9,896)


(9,955)

Total operating expense


(46,096)


(51,497)

Loss from operations


(25,245)


(28,464)






Other income (expense)





Interest income


1,994


2,054

Interest expense


(12,349)


(12,230)

Other, net


2,632


203

Total other expense, net


(7,723)


(9,973)

Loss before income taxes


(32,968)


(38,437)

Income tax expense



(165)

Net loss


$       (32,968)


$      (38,602)






Net loss per share





Net loss per share, basic and diluted


$           (0.21)


$          (0.36)

Weighted average shares outstanding, basic and diluted


154,142,347


107,202,374

 

ADC Therapeutics SA

Condensed Consolidated Balance Sheets (Unaudited)

(in thousands)




March 31, 2026


December 31, 2025

ASSETS





Current assets





Cash and cash equivalents


$         231,008


$         261,338

Accounts receivable, net


31,045


29,117

Inventory


4,776


4,184

Prepaid expenses


5,674


5,612

Other current assets


4,265


6,084

Total current assets


276,768


306,335

Non-current assets





Inventory, long-term


12,282


14,301

Operating lease right-of-use assets


1,200


1,297

Other long-term assets


1,246


1,217

Total assets


$         291,496


$         323,150






LIABILITIES AND SHAREHOLDERS' (DEFICIT) EQUITY





Current liabilities





Accounts payable


$             5,295


$             9,175

Accrued expenses and other current liabilities


57,698


57,988

Senior secured term loans, current portion


4,635


3,000

Total current liabilities


67,628


70,163






Deferred royalty obligation, long-term


304,687


322,525

Senior secured term loans, long-term


111,042


112,452

Warrant obligations


18,527


Operating lease liabilities, long-term


991


1,034

Other long-term liabilities


4,998


2,810

Total liabilities


507,873


508,984






Total shareholders' (deficit) equity


(216,377)


(185,834)






Total liabilities and shareholders' (deficit) equity


$         291,496


$         323,150

 

ADC Therapeutics SA

Reconciliation of GAAP Measures to Non-GAAP Measures (Unaudited)

(in thousands, except for share and per share data)



Three Months Ended March 31,

(in thousands)

2026


2025


Change


%
Change

Total operating expense

$ (46,096)


$ (51,497)


$  5,401


(10) %

Adjustments:








Share-based compensation expense (i)

3,209


2,421


788


33 %

Adjusted total operating expenses

$ (42,887)


$ (49,076)


$  6,189


(13) %

 


Three Months Ended
March 31,

in thousands (except for share and per share data)

2026


2025

Net loss

$      (32,968)


$     (38,602)

Adjustments:




Share-based compensation expense (i)

3,209


2,421

HCR warrants obligation, change in fair value income (ii)

(2,227)


Effective interest expense on senior secured term loan facility (iii)

3,622


3,785

Deferred royalty obligation interest expense (iv)

8,727


8,445

Deferred royalty obligation cumulative catch-up adjustment income (iv)

(72)


(12)

Adjusted net loss

$      (19,709)


$     (23,963)

Net loss per share, basic and diluted

$          (0.21)


$         (0.36)

Adjustment to net loss per share, basic and diluted

0.08


0.14

Adjusted net loss per share, basic and diluted

$          (0.13)


$         (0.22)

Weighted average shares outstanding, basic and diluted

154,142,347


107,202,374

(i)

Share-based compensation expense represents the cost of equity awards issued to our directors, management and employees. The fair value of awards is computed at the time the award is granted and is recognized over the requisite service period less actual forfeitures by a charge to the statement of operations and a corresponding increase in additional paid-in capital within equity. These accounting entries have no cash impact.



(ii)

Change in the fair value of the HCR warrants obligation results from the valuation at the end of each accounting period. There are several inputs to these valuations, but those most likely to result in significant changes to the valuations are changes in the value of the underlying instrument (i.e., changes in the price of our common shares) and changes in expected volatility in that price. These accounting entries have no cash impact.



(iii)

Effective interest expense on senior secured term loans relates to the increase in the value of our loans in accordance with the amortized cost method.



(iv)

Deferred royalty obligation interest expense relates to the accretion expense on our deferred royalty obligation pursuant to the royalty purchase agreement with HCR and cumulative catch-up adjustments related to changes in the expected payments to HCR based on a periodic assessment of our underlying revenue projections.

CONTACT:
Investors and Media
Nicole Riley
ADC Therapeutics
Nicole.Riley@adctherapeutics.com 
+1 862-926-9040

Cision View original content to download multimedia:https://www.prnewswire.com/news-releases/adc-therapeutics-reports-first-quarter-2026-financial-results-and-provides-operational-updates-302760423.html

SOURCE ADC Therapeutics SA

FAQ

When will ADC Therapeutics (ADCT) report LOTIS-5 results and what comes next?

Topline LOTIS-5 Phase 3 results are expected in 2Q 2026. According to the company, full LOTIS-5 data and LOTIS-7 results are anticipated by year-end, with a potential sBLA submission before year-end if results are positive.

What were ADCT's Q1 2026 revenues and how did they change year-over-year?

Q1 2026 net product revenue was $20.0 million, up from $17.4 million in Q1 2025. According to the company, the increase was driven primarily by higher volume and pricing variability in customer orders.

How much cash did ADC Therapeutics (ADCT) report at March 31, 2026 and how long will it last?

Cash and cash equivalents were $231.0 million as of March 31, 2026. According to the company, this provides an expected cash runway at least into 2028.

What were ADCT's reported net loss and adjusted net loss for Q1 2026?

Net loss for Q1 2026 was $33.0 million (loss of $0.21 per share). According to the company, adjusted net loss was $19.7 million (adjusted loss of $0.13 per share).

What operational milestones could affect ADCT's stock in 2026?

Near-term catalysts include LOTIS-5 topline in 2Q 2026 and full LOTIS-5/7 data by year-end. According to the company, positive results could lead to an sBLA submission before year-end and regulatory pathways in 2027.