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
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Every filing, read
last 12 months · SECWhat 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
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
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 · Q2-2026 | 17.0% |
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.”
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.”
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 · Q2-2026 | 17.0% | |
| 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
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-5 | 58.1% | |
| complete response rate · test arm · LOTIS-5 | 39.5% | |
| 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.”
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”
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
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 |
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
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
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_time | 9,834,776 |
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.”
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
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 · Q4-2025 | 89.8% | |
| complete response rate · r/r DLBCL · Q4-2025 | 77.6% |
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
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.”
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
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.