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ADC Therapeutics SA (ADCT) SEC Filings & Earnings Calls

EquiReason read 17 ADC Therapeutics SA SEC filings in the last 12 months. Latest: 8-K on 2026-10-13 — ADC Therapeutics SA announced an $86.6M PIPE, amended HCR royalty agreement to remove $150M change-of-control payment, and refinanced senior loan to $50M with bullet payment in 202.

Source: SEC EDGAR filings · figures as of 2026-06-30 · read by EquiReason

ADCTADC Therapeutics SAFollow ADCT — free
Biotechnology · Healthcare
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Price chart with a free account
Market cap
183.8M
P/E TTM
—
Dividend yield
—
52-week
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Next earnings
10 Nov, in 17 days

Every filing, read

last 12 months · SEC

What happened, the numbers inside, guidance and risks. The original is one click away.

13 Oct 20268-K · 1.01, 2.02, 3.02ADC Therapeutics SA announced an $86.6M PIPE, amended HCR royalty agreement to remove $150M change-of-control payment, and refinanced senior loan to $50M with bullet payment in 2029, extending cash runway into 2029.open

Risks flagged

Preliminary financial results are unaudited and subject to material adjustments.

“The preliminary financial information is not a comprehensive statement... Subsequent information or events may lead to material differences” · word for word

Shareholder dilution from PIPE and warrant exercises.

“selling 12.9 million common shares at $1.42 per share and pre-funded warrants to purchase 48.1 million common shares” · word for word
Read the original on SEC EDGAR ↗
13 Aug 202610-QFDA expressed substantial concerns about LOTIS-5 trial benefit-risk profile due to Grade 5 event imbalance, potentially preventing label expansion and threatening existing accelerated approval.open

Figures in the filing · each found in the filing text

Product revenues, net · Q2-2026$19M+3% y/y
Total revenue, net · Q2-2026$19M+2% y/y
Research and development expense · Q2-2026$17M-42% y/y
Net loss · Q2-2026$-17M-71% y/y
Net loss per share, basic and diluted · Q2-2026$-0.11-78% y/y

Risks flagged

Regulatory risk - potential withdrawal of accelerated approval

“The FDA noted substantial concerns regarding the benefit-risk or verification of clinical benefit observed in this trial based on the imbalance in Grade 5 events, when assessed in the context of a marginal treatment benefit.” · word for word

Clinical trial safety signal

“A higher rate of Grade 5 TEAEs was observed in the ZYNLONTA plus rituximab arm (27 pts/13.2%) vs. R-GemOx (9 pts/4.6%).” · word for word

Restructuring execution risk

“We are reducing our global workforce by approximately 17%, which is expected to be substantially completed by September 30, 2026.” · word for word

Revenue concentration on single product

“We generate product revenue through the sale of ZYNLONTA in the United States.” · word for word
Read the original on SEC EDGAR ↗
13 Aug 20268-K · 2.02, 7.01Net Product Revenue $19M; Cash and Cash Equivalents $219M; Annualized Cost Savings from Restructuring $10Mearningsopen

Figures in the filing · each found in the filing text

Net Product Revenue · Q2-2026$19M
Cash and Cash Equivalents · Q2-2026$219M
Annualized Cost Savings from Restructuring · FY2026$10M
Workforce Reduction · Q2-202617.0%

Risks flagged

FDA regulatory setback for LOTIS-5; potential delay or denial of full approval.

“FDA pre-sBLA meeting noted 'substantial concerns regarding the benefit-risk' and 'marginal treatment benefit'.”

Dependence on ZYNLONTA as sole commercial product; limited pipeline diversification.

“Net product revenue entirely from ZYNLONTA; LOTIS-7 and MZL IIT data pending.”

Restructuring execution risk; workforce reduction may impact morale and capabilities.

“17% workforce reduction; $10M annual savings target.”
Read the original on SEC EDGAR ↗
2 Jul 20268-K · 5.02Reported a director or officer change (departure, election, appointment or pay arrangement)open

Risks flagged

Key person retention risk mitigated via awards; potential cash outflow if executives leave before June 2027.

“Cash portion subject to repayment if employment terminates before June 30, 2027.”
Read the original on SEC EDGAR ↗
24 Jun 20268-K · 7.01, 8.01Workforce reduction percentage 17; annualized cost savings $10M; restructuring charges $3Mopen

Figures in the filing · each found in the filing text

workforce reduction percentage · Q2-202617.0%
annualized cost savings · FY2027$10M
restructuring charges · Q2-2026$3M

Risks flagged

Execution risk on achieving cost savings; potential additional costs not currently contemplated.

“Company may also incur additional costs not currently contemplated due to events that may occur as a result of, or that are associated with, the reduction.” · word for word
Read the original on SEC EDGAR ↗
3 Jun 20268-K · 7.01, 8.01Progression-free survival hazard ratio 0.73; median progression-free survival 6.1; overall response rate 58.1open

Figures in the filing · each found in the filing text

progression-free survival hazard ratio · LOTIS-5$0.73
median progression-free survival · test arm · LOTIS-5$6.10
overall response rate · test arm · LOTIS-558.1%
complete response rate · test arm · LOTIS-539.5%
median duration of response · test arm · LOTIS-5$9.20
median duration of complete response · test arm · LOTIS-5$16.80
overall survival hazard ratio · LOTIS-5$0.96

Risks flagged

Safety signal: higher Grade 5 TEAEs and SAEs in test arm, particularly in elderly patients.

“Higher rates of serious adverse events were seen in the test arm (49.0% vs. 34.5%). A higher rate of Grade 5 TEAEs was observed in the ZYNLONTA plus rituximab arm (27 pts/13.2%) vs. R-GemOx (9 pts/4.6%).”

Regulatory risk: sBLA submission and approval not guaranteed; FDA feedback pending.

“Company plans to conduct a pre-sBLA meeting with FDA in August and is preparing for a planned sBLA submission in Q4 2026.”
Read the original on SEC EDGAR ↗
4 May 202610-QProduct revenues, net $20M (+15% y/y); Total revenue, net $21M (-10% y/y); Net loss $-33M (+15% y/y)open

Figures in the filing · each found in the filing text

Product revenues, net · Q1-2026$20M+15% y/y
Total revenue, net · Q1-2026$21M-10% y/y
Net loss · Q1-2026$-33M+15% y/y
Cash and cash equivalents · 2026-03-31$231M+19% y/y
Research and development expense · Q1-2026$20M-31% y/y
Cost of product sales · Q1-2026$4M+75% y/y
Net cash used in operating activities · Q1-2026$-30M+47% y/y
Deferred royalty obligation, long-term · 2026-03-31$305M

Risks flagged

High debt and royalty obligation burden

“Deferred royalty obligation, long-term $304,687k and Senior secured term loans, long-term $111,042k”

Negative equity and accumulated deficit

“Total shareholders’ (deficit) equity $(216,377)k and Accumulated deficit $(1,668,909)k”

Dependence on single product ZYNLONTA

“The Company generates sales from its flagship product, ZYNLONTA” · word for word

Customer concentration risk

“AmerisourceBergen Corporation 39%, McKesson 36%, Cardinal Health 25% of product revenues”
Read the original on SEC EDGAR ↗
4 May 20268-K · 2.02Net product revenues $20M (+15% y/y); License revenues and royalties $800,000.00; Cost of product sales $4Mearningsopen

Figures in the filing · each found in the filing text

Net product revenues · Q1-2026$20M+15% y/y
License revenues and royalties · Q1-2026$800000.00
Cost of product sales · Q1-2026$4M
Research and Development Expense · Q1-2026$20M
Selling and Marketing Expense · Q1-2026$13M
General & Administrative Expense · Q1-2026$10M
Net loss · Q1-2026$-33M
Cash and cash equivalents · Q1-2026$231M

Risks flagged

Clinical trial risk: LOTIS-5 and LOTIS-7 data readouts are binary catalysts; failure could impair growth trajectory.

“LOTIS-5 Phase 3 topline data expected in second quarter 2026; full data for LOTIS-5 and LOTIS-7 anticipated by year end.” · word for word

Revenue concentration on ZYNLONTA; dependence on label expansion for growth.

“Net product revenues were $20.0 million; pipeline expansion needed for sustained growth.” · word for word
Read the original on SEC EDGAR ↗
20 Apr 2026DEF 14AZynlonta net sales $74M (+6% y/y)open

Figures in the filing · each found in the filing text

Zynlonta net sales · Zynlonta · FY2025$74M+6% y/y
Read the original on SEC EDGAR ↗
10 Mar 20268-K · 2.02Net product revenue $22M (+36% y/y); Net product revenue $74M (+6% y/y); Cash and cash equivalents $261Mearningsopen

Figures in the filing · each found in the filing text

Net product revenue · Q4-2025$22M+36% y/y
Net product revenue · FY2025$74M+6% y/y
Cash and cash equivalents · Q4-2025$261M
R&D expense · Q4-2025$18M
R&D expense · FY2025$104M

Risks flagged

Restructuring costs of $13.1M in FY2025 related to strategic reprioritization.

“The Company incurred $0.3 million in income for the fourth quarter and $13.1 million in restructuring, impairment and other related costs for the full year ended December 31, 2025” · word for word
Read the original on SEC EDGAR ↗
10 Mar 202610-KProduct revenues, net $74M (+6% y/y); Total revenue, net $81M (+15% y/y); Net loss $-143M (-10% y/y)open

Figures in the filing · each found in the filing text

Product revenues, net · FY2025$74M+6% y/y
Total revenue, net · FY2025$81M+15% y/y
Net loss · FY2025$-143M-10% y/y
Research and development expense · FY2025$104M-5% y/y
Selling and marketing expense · FY2025$43M-2% y/y
General and administrative expense · FY2025$37M-13% y/y
License revenues and royalties · FY2025$8M+401% y/y
Cost of product sales · FY2025$6M-3% y/y
Interest income · FY2025$9M-28% y/y
Interest expense · FY2025$52M+3% y/y

Risks flagged

Single product dependency

“We generate product revenue through the sale of ZYNLONTA in the United States.” · word for word

Restructuring execution risk

“The Company closed down its UK facility, and has reduced its global workforce across functions by approximately 30%.” · word for word

Patent expiration risk

“Even if patents covering our product candidates are obtained, once the patent life has expired for a product, we may be open to competition from competitive medications, including biosimilar medications.” · word for word
Read the original on SEC EDGAR ↗
23 Feb 20268-K · 1.01, 3.02ADC Therapeutics amended royalty purchase agreement with HCR, reducing change-of-control payment but issuing dilutive warrants for 9.8M shares at $3.8130. Increases potential dilution and modifies debt-like obligation.open

Figures in the filing · each found in the filing text

funding from HCR · point_in_time$300M
change-of-control payment (original) · point_in_time$750M
change-of-control payment (amended, before 2028) · point_in_time$150M
change-of-control payment (amended, after 2028) · point_in_time$200M
royalty buyout amount (before 2030) · point_in_time$525M
royalty buyout amount (after 2030) · point_in_time$750M
warrant exercise price · point_in_time$3.81
warrant shares issued · point_in_time9,834,776

Risks flagged

Significant shareholder dilution from warrant issuance; potential further dilution if warrants are exercised.

“Issued warrants for 9.8M shares at $3.813, representing ~10% of current shares (assuming ~100M shares outstanding).”

Increased financial obligations post-change-of-control; royalty buyout amounts are substantial relative to company size.

“Royalty buyout of $525M-$750M, plus change-of-control payment, could exceed company's market cap.”
Read the original on SEC EDGAR ↗
12 Jan 20268-K · 7.01Issued a Regulation FD disclosure (forward guidance or material update); filed financial statements and exhibits with this reportSEC ↗
8 Jan 20268-K · 2.02, 7.01Net product revenue $73M (+5% y/y); Net product revenue $22M (+34% y/y); Cash and cash equivalents $261Mearningsopen

Figures in the filing · each found in the filing text

Net product revenue · ZYNLONTA · FY2025$73M+5% y/y
Net product revenue · ZYNLONTA · Q4-2025$22M+34% y/y
Cash and cash equivalents · Q4-2025$261M

Risks flagged

Preliminary and unaudited results; subject to change.

“The revenue and cash and cash equivalents figures are preliminary and unaudited.” · word for word
Read the original on SEC EDGAR ↗
5 Dec 20258-K · 8.01Overall response rate 89.8; complete response rate 77.6open

Figures in the filing · each found in the filing text

overall response rate · r/r DLBCL · Q4-202589.8%
complete response rate · r/r DLBCL · Q4-202577.6%

Risks flagged

Clinical trial data is early-stage; safety includes Grade 5 AEs in 2 patients.

“Grade 5 AEs occurred in 2 (4.1%) patients.” · word for word
Read the original on SEC EDGAR ↗
10 Nov 20258-K · 2.02Net product revenue $16M (-12% y/y); Net loss $-41M (+7% y/y); R&D expense $27M (-18% y/y)earningsopen

Figures in the filing · each found in the filing text

Net product revenue · Q3-2025$16M-12% y/y
Net loss · Q3-2025$-41M+7% y/y
R&D expense · Q3-2025$27M-18% y/y

Risks flagged

Revenue decline and continued net losses indicate commercial challenges.

“Net product revenue down 12% YoY; net loss of $41M.”

Dependence on clinical trial outcomes for future growth.

“LOTIS-5 topline results expected in 1H 2026; regulatory approval risk.”
Read the original on SEC EDGAR ↗
10 Nov 202510-QProduct revenues, net $16M (-13% y/y); Total revenue, net $16M (-11% y/y); Net loss $-41M (-7% y/y)open

Figures in the filing · each found in the filing text

Product revenues, net · Q3-2025$16M-13% y/y
Total revenue, net · Q3-2025$16M-11% y/y
Net loss · Q3-2025$-41M-7% y/y
Research and development expenses · Q3-2025$27M-18% y/y
Cash and cash equivalents · Q3-2025$235M

Risks flagged

Tariff cost pressure

“We operate internationally and our products are manufactured outside of the United States, primarily in Europe. As a result, we may experience higher costs of sales and increased operating expenses in the future due to tariffs that may be imposed on U.S imports of our product for commercial sale in the U.S.” · word for word

Drug pricing policy risk

“if MFN drug pricing is implemented, the U.S. list price of ZYNLONTA that is also being commercialized outside of the United States could be substantially reduced, which could negatively impact our U.S. product sale revenues and the overall U.S. market opportunity.” · word for word
Read the original on SEC EDGAR ↗

ADC Therapeutics SA — questions

What did ADC Therapeutics SA file recently?
17 SEC filings in the last 12 months. Latest: 8-K on 2026-10-13 — ADC Therapeutics SA announced an $86.6M PIPE, amended HCR royalty agreement to remove $150M change-of-control payment, and refinanced senior loan to $50M with bullet payment in 2029, extending cash runway into 2029.

Every figure on this page comes from ADC Therapeutics SA's own SEC filings — see them on SEC EDGAR. Price data is licensed and shown only inside the product.

How these figures are read: methodology · EquiReason.