- Clinical responses with ADP-A2M4 in 7 out of 12 patients with synovial sarcoma, and clinical benefit in 11 out of 12 patients -
- ADP-A2M4 granted Orphan Drug Designation for treatment of soft tissue sarcomas -
- Enrolling across SPEARHEAD-1 and SURPASS trials at multiple sites -
-
- Progressed to third cohort in ADP-A2AFP trial in liver cancer -
-
- Financial guidance confirmed: funded through Q3 2020 -
- Conference call to be held today at
“The sarcoma community has been very supportive following the
COMMERCIAL READINESSS FOR ADP-A2M4 IN SARCOMA WITH AIM TO LAUNCH IN 2022
- Data presented at
ESMO 2019 demonstrating a clear benefit of ADP-A2M4 for patients with synovial sarcoma showing:
º Overall response rate of 58% with 7 out of 12 evaluable patients with clinical responses
º Disease control rate (best overall responses of partial response or stable disease) of 92% with 11 out of 12 evaluable patients showing clinical benefit
º These data will be updated at CTOS onNovember 16 th - Enrolling patients in SPEARHEAD-1 (Phase 2 trial in synovial sarcoma and myxoid/ round cell liposarcoma) across several leading clinical trial centers
- US
FDA granted Orphan Drug Designation to SPEAR T-cells targeting MAGE-A4 (the ADP-A2M4 program) for the treatment of soft tissue sarcomas - Produced first in-house GMP viral vector batch, augmenting the Company’s external supply with internal manufacturing capabilities
FOCUSED ON EXECUTION IN OTHER CLINICAL TRIALS
- Dosing in the SURPASS trial with ADP-A2M4CD8 – the first next-generation trial at several clinical trial centers with data updates anticipated in 1H 2020
º Preclinical data show that these next-generation SPEAR T-cells may improve long term T‑cell function as well as antitumor activity - Enrolling in Cohort 3 in the ADP-A2AFP trial in liver cancer at target doses of 5 billion SPEAR T‑cells (range 1.2 to 6 billion), after Safety Review Committee endorsed dose escalation
- Continuing enrollment in the radiation sub-study of the Phase
1 ADP -A2M4 trial - Based on emerging translational data to be presented at
SITC onNovember 8 th, will initiate a clinical trial combining ADP-A2M4 with a PD-1 pathway inhibitor in 2020
PRECLINICAL
- Continued progress with stem-cell derived allogeneic program, which is applicable to all T-cells (including both CAR-T and TCR T-cells) with data updates next year
- Initiated collaboration with Noile-Immune to develop further next-generation products
OTHER CORPORATE NEWS
Michael Garone appointed as Interim Chief Financial Officer- The Company is recruiting for a permanent Chief Medical Officer and Chief Financial Officer
Financial Results for the three-month period ended
- Cash / liquidity position: As of
September 30, 2019 , Adaptimmune had cash and cash equivalents of$39.4 million and Total Liquidity1 of$102.9 million . The Company also received$15.8 million for UK R&D Tax Credits inOctober 2019 .
- Revenue: Revenue for the three and nine months ended
September 30, 2019 was$0.2 million and$0.4 million respectively, compared to$40.8 million and$58.0 million for the same periods in 2018. The revenue in the three and nine months ended 2019 is due to the commencement of development under the third target nominated by GSK under the Collaboration and License Agreement, whereas the development and license revenue for the same periods in 2018 was recognized due to the performance under the NY-ESO transition program and the PRAME development plan, which were completed in 2018.
- Research and development (R&D) expenses: R&D expenses for the three and nine months ended September 30, 2019 were
$29.6 million and$77.1 million , respectively, compared to$23.5 million and$75.5 million for the same periods of 2018. The three and nine month periods endedSeptember 30, 2019 include the impact of recognized purchase commitments for clinical materials of$5.0 million , and in process research and development payments relating to the collaboration agreements withAlpine Immune Sciences, Inc of$2.0 million inMay 2019 andNoile-Immune Biotech, Inc of$2.5 million inAugust 2019 . These increases were partially offset by a decrease in share-based compensation expense due to option forfeitures in both periods, an increase in reimbursements for research and development tax and expenditure credits in both periods, and, during the nine months endedSeptember 30, 2019 , a reduction in expenditure associated with the NY-ESO program, which was transferred to GSK on July 23, 2018.
- General and administrative (G&A) expenses: G&A expenses for the three and nine months ended September 30, 2019 were
$10.7 million and$32.7 million respectively, compared to$10.3 million and$32.8 million for the same periods of 2018.
- Other income (expense), net: Other income (expense), net for the three and nine months ended
September 30, 2019 was income of$0.3 million and an expense of$0.6 million respectively, compared to expenses of$2.2 million and$10.5 million for the same periods of 2018. Other income (expense), net primarily comprises unrealized foreign exchange losses, which fluctuate depending on exchange rate movements and the amount of foreign currency assets and liabilities. Management determined that, effective fromJuly 1, 2019 , an intercompany loan was of a long-term investment nature and therefore, from that date, foreign exchange differences on this intercompany loan have subsequently been reported within other comprehensive income (loss).
- Net (loss) income: Net (loss) income attributable to holders of the Company’s ordinary shares for the three and nine month periods ended
September 30, 2019 was losses of$39.3 million and$107.8 million respectively, and$(0.06) and$(0.17) per ordinary share respectively, compared to income of$5 .2 million and a loss of$59.3 million respectively, and$0.01 and$(0.10) per ordinary share respectively in the same periods of 2018.
Financial guidance
The Company believes that its existing cash, cash equivalents and marketable securities will fund the Company’s current operations through the third quarter of 2020. As further detailed in the Company’s Quarterly Report on Form 10-Q for the fiscal quarter ended
Conference Call and Webcast Information
The Company will host a live teleconference at 8:00 a.m. EST (
About Adaptimmune
Adaptimmune is a clinical-stage biopharmaceutical company focused on the development of novel cancer immunotherapy products for cancer patients. The Company’s unique SPEAR (Specific Peptide Enhanced Affinity Receptor) T‑cell platform enables the engineering of T-cells to target and destroy cancer across multiple solid tumors. For more information, please visit http://www.adaptimmune.com.
1 Total liquidity is a non-GAAP financial measure, which is explained and reconciled to the most directly comparable financial measures prepared in accordance with GAAP below.
Forward-looking statements
This release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995 (PSLRA). These forward-looking statements involve certain risks and uncertainties. Such risks and uncertainties could cause our actual results to differ materially from those indicated by such forward-looking statements, and include, without limitation: the success, cost and timing of our product development activities and clinical trials and our ability to successfully advance our TCR therapeutic candidates through the regulatory and commercialization processes. For a further description of the risks and uncertainties that could cause our actual results to differ materially from those expressed in these forward-looking statements, as well as risks relating to our business in general, we refer you to our Quarterly Report on Form 10-Q filed with the
Total Liquidity (a non-GAAP financial measure)
Total Liquidity (a non-GAAP financial measure) is the total of cash and cash equivalents and marketable securities. Each of these components appears in the consolidated balance sheet. The U.S. GAAP financial measure most directly comparable to Total Liquidity is cash and cash equivalents as reported in the consolidated financial statements, which reconciles to Total Liquidity as follows (in thousands):
September 30, | December 31, | ||||
2019 | 2018 | ||||
Cash and cash equivalents | $ | 39,409 | $ | 68,379 | |
Marketable securities | 63,451 | 136,755 | |||
Total Liquidity | $ | 102,860 | $ | 205,134 | |
The Company believes that the presentation of Total Liquidity provides useful information to investors because management reviews Total Liquidity as part of its management of overall liquidity, financial flexibility, capital structure and leverage.
Condensed Consolidated Statement of Operations
(unaudited, in thousands, except per share data)
Three months ended | Nine months ended | ||||||||||||||
September 30, | September 30, | ||||||||||||||
2019 | 2018 | 2019 | 2018 | ||||||||||||
Development revenue | 237 | 1,678 | 394 | 18,912 | |||||||||||
License revenue | — | 39,114 | — | 39,114 | |||||||||||
Total revenue | $ | 237 | $ | 40,792 | $ | 394 | $ | 58,026 | |||||||
Operating expenses | |||||||||||||||
Research and development (including losses accrued on firm purchase commitments of $5,000, $-, $5,000 and $-) | (29,617 | ) | (23,484 | ) | (77,147 | ) | (75,500 | ) | |||||||
General and administrative | (10,741 | ) | (10,290 | ) | (32,662 | ) | (32,785 | ) | |||||||
Total operating expenses | (40,358 | ) | (33,774 | ) | (109,809 | ) | (108,285 | ) | |||||||
Operating (loss) income | (40,121 | ) | 7,018 | (109,415 | ) | (50,259 | ) | ||||||||
Interest income | 615 | 606 | 2,324 | 1,805 | |||||||||||
Other income (expense), net | 291 | (2,249 | ) | (556 | ) | (10,525 | ) | ||||||||
(Loss) income before income taxes | (39,215 | ) | 5,375 | (107,647 | ) | (58,979 | ) | ||||||||
Income taxes | (87 | ) | (133 | ) | (154 | ) | (362 | ) | |||||||
Net (loss) income attributable to ordinary shareholders | $ | (39,302 | ) | $ | 5,242 | $ | (107,801 | ) | $ | (59,341 | ) | ||||
Net (loss) income per ordinary share - Basic and diluted | |||||||||||||||
Basic | $ | (0.06 | ) | $ | 0.01 | $ | (0.17 | ) | $ | (0.10 | ) | ||||
Diluted | (0.06 | ) | 0.01 | (0.17 | ) | (0.10 | ) | ||||||||
Weighted average shares outstanding: | |||||||||||||||
Basic | 630,866,800 | 582,004,954 | 629,403,293 | 573,796,275 | |||||||||||
Diluted | 630,866,800 | 621,764,201 | 629,403,293 | 573,796,275 | |||||||||||
Condensed Consolidated Balance Sheets
(unaudited, in thousands, except share data)
September 30, | December 31, | ||||||
2019 | 2018 | ||||||
Assets | |||||||
Current assets | |||||||
Cash and cash equivalents | $ | 39,409 | $ | 68,379 | |||
Marketable securities - available-for-sale debt securities | 63,451 | 136,755 | |||||
Accounts receivable, net of allowance for doubtful accounts of $0 and $0 | — | 192 | |||||
Other current assets and prepaid expenses (including current portion of clinical materials) | 44,110 | 25,769 | |||||
Total current assets | 146,970 | 231,095 | |||||
Restricted cash | 4,318 | 4,097 | |||||
Clinical materials | 2,485 | 3,953 | |||||
Operating lease right-of-use assets, net of accumulated amortization | 20,563 | — | |||||
Property, plant and equipment, net of accumulated depreciation of $20,818 (2018: $15,924) | 31,641 | 36,118 | |||||
Intangibles, net of accumulated amortization | 2,274 | 1,473 | |||||
Total assets | $ | 208,251 | $ | 276,736 | |||
Liabilities and stockholders’ equity | |||||||
Current liabilities | |||||||
Accounts payable | 5,535 | 4,083 | |||||
Operating lease liabilities, current | 2,337 | — | |||||
Accrued expenses and other accrued liabilities | 26,846 | 20,354 | |||||
Deferred revenue | 2,683 | — | |||||
Total current liabilities | 37,401 | 24,437 | |||||
Operating lease liabilities, non-current | 22,599 | — | |||||
Other liabilities, non-current | 568 | 5,414 | |||||
Total liabilities | 60,568 | 29,851 | |||||
Stockholders’ equity | |||||||
Common stock - Ordinary shares par value £0.001, 785,857,300 authorized and 630,952,736 issued and outstanding (2018: 701,103,126 authorized and 627,454,270 issued and outstanding) | 943 | 939 | |||||
Additional paid in capital | 583,065 | 574,208 | |||||
Accumulated other comprehensive loss | (10,025 | ) | (9,763 | ) | |||
Accumulated deficit | (426,300 | ) | (318,499 | ) | |||
Total stockholders' equity | 147,683 | 246,885 | |||||
Total liabilities and stockholders’ equity | $ | 208,251 | $ | 276,736 | |||
Condensed Consolidated Cash Flow Statement
(unaudited, in thousands)
Nine months ended | |||||||
September 30, | |||||||
2019 | 2018 | ||||||
Cash flows from operating activities | |||||||
Net loss | $ | (107,801 | ) | $ | (59,341 | ) | |
Adjustments to reconcile net loss to net cash used in operating activities: | |||||||
Depreciation | 5,406 | 5,248 | |||||
Amortization | 511 | 464 | |||||
Share-based compensation expense | 8,495 | 12,453 | |||||
Realized (gain) loss on available-for-sale debt securities | (13 | ) | 2,473 | ||||
Unrealized foreign exchange losses | 522 | 4,921 | |||||
Other | (195 | ) | 262 | ||||
Changes in operating assets and liabilities: | |||||||
Increase in receivables and other operating assets | (20,075 | ) | (4,140 | ) | |||
Decrease in non-current operating assets | 1,468 | 490 | |||||
Increase (decrease) in payables and deferred revenue | 11,703 | (35,533 | ) | ||||
Net cash used in operating activities | (99,979 | ) | (72,703 | ) | |||
Cash flows from investing activities | |||||||
Acquisition of property, plant and equipment | (1,425 | ) | (3,823 | ) | |||
Acquisition of intangibles | (1,036 | ) | (666 | ) | |||
Maturity or redemption of marketable securities | 92,803 | 114,988 | |||||
Investment in marketable securities | (19,080 | ) | (75,545 | ) | |||
Net cash provided by investing activities | 71,262 | 34,954 | |||||
Cash flows from financing activities | |||||||
Proceeds from issuance of common stock, net of issuance costs of $0 and $347 | — | 99,653 | |||||
Proceeds from exercise of stock options | 366 | 2,933 | |||||
Net cash provided by financing activities | 366 | 102,586 | |||||
Effect of currency exchange rate changes on cash, cash equivalents and restricted cash | (398 | ) | 4,111 | ||||
Net (decrease) increase in cash and cash equivalents | (28,749 | ) | 68,948 | ||||
Cash, cash equivalents and restricted cash at start of period | 72,476 | 88,296 | |||||
Cash, cash equivalents and restricted cash at end of period | $ | 43,727 | $ | 157,244 | |||
Adaptimmune Contacts:
Media Relations:
Sébastien Desprez — VP, Communications and Investor Relations
T: +44 1235 430 583
M: +44 7718 453 176
Sebastien.Desprez@adaptimmune.com
Investor Relations:
T: +1 215 825 9310
M: +1 215 460 8920
Juli.Miller@adaptimmune.com
Source: Adaptimmune Therapeutics plc