Adaptimmune Reports First Quarter 2016 Financial Results
PHILADELPHIA and OXFORD, United Kingdom, May 12, 2016 (GLOBE NEWSWIRE) -- Adaptimmune Therapeutics plc (Nasdaq:ADAP) (“Adaptimmune” or the “Company”), a leader in T-cell therapy to treat cancer, today reported financial results for the first quarter ended March 31, 2016.
As of March 31, 2016, Adaptimmune had a total liquidity position1 of $226.1 million. The Company is reiterating its cash burn guidance and expects its total liquidity position at December 31, 2016, including cash, cash equivalents and short term deposits, to be at least $150 million.
“As we described at our Investor and Analyst meeting in April, we have made substantial progress toward our goal of delivering the first affinity optimized T-cell therapy to market,” commented James Noble, Adaptimmune’s Chief Executive Officer. “The first quarter of 2016 was marked by strong momentum as we continued development of our comprehensive pipeline of SPEAR™ T-cell therapies covering solid and hematologic cancers. In addition to our ongoing clinical activities, we received orphan drug designation and breakthrough therapy designation for our NY-ESO SPEAR T-cell therapy. We also opened our IND for our therapeutic candidate targeting AFP in liver cancer and announced MAGE-A4 as our next target with the goal of achieving IND acceptance in 2017.”
Recent Corporate and Clinical Highlights:
- Hosted inaugural Investor and Analyst Day on April 22, 2016;
- Received orphan drug designation from U.S. Food and Drug Administration (“FDA”) for NY-ESO SPEAR T-cell therapy in soft tissue sarcoma;
- Received breakthrough therapy designation from FDA for NY-ESO SPEAR T-cell therapy in synovial sarcoma;
- Received FDA acceptance of investigational new drug (“IND”) application for AFP SPEAR T-cell therapy in liver cancer;
- Announced that the Company’s next IND would be for its MAGE-A4 SPEAR T-cell therapy, with the goal of achieving IND acceptance in 2017;
- Announced update on NY-ESO SPEAR T-cell data in patients with multiple myeloma, including a 90 percent response rate in conjunction with autologous stem cell transplant and median overall survival of approximately three years (as of January 2016);
- Filed patents on over 60 targets expressed on multiple cancers;
- Presented overview of commercial-ready manufacturing process, including progress toward opening of manufacturing facility in 2017;
- Expanded terms of strategic collaboration agreement with GSK in February 2016 to accelerate Adaptimmune’s lead clinical cancer program, a SPEAR T-cell therapy targeting NY-ESO, with goal of initiating pivotal trials in 4Q16/1Q17;
- Established Scientific Advisory Board of leading immunotherapy experts; and
- Adopted brand of SPEAR (Specific Peptide Enhanced Affinity Receptor) T-cells to describe proprietary technology that uniquely delivers correctly identified targets and enhanced affinity T-cell receptors with potency to attack tumors, but optimum specificity to minimize risks of cross-reactivity.
Financial Results for the three-month period ended March 31, 2016
- Cash / liquidity position: As of March 31, 2016, Adaptimmune had a total liquidity position of $226.1 million, consisting of $163.8 million of cash and cash equivalents and $62.3 million of short-term deposits. As of December 31, 2015, Adaptimmune had a total liquidity position of $248.9 million, consisting of $194.3 million of cash and cash equivalents and $54.6 million of short-term deposits.
- Cash burn: The net decrease in the total liquidity position was $22.8 million for the three months ended March 31, 2016, consisting of a $30.5 million decrease in cash and cash equivalents and a $7.7 million increase in short-term deposits.
- Revenue: For the three months ended March 31, 2016, revenue was $2.9 million compared to $2.7 million for the three months ended March 31, 2015. This increase was primarily due to revenue relating to development milestones related to the GSK Collaboration and License Agreement achieved in August and December 2015, which is being recognized over the period in which we are delivering services.
- Research and development (“R&D”) expenses: R&D expenses increased to $13.9 million for the three months ended March 31, 2016 from $6.0 million for the three months ended March 31, 2015, primarily due to increased period-over-period costs associated with: ongoing clinical trials of the Company’s NY-ESO and MAGE-A10 SPEAR T-cell therapies; preparation for a study with the Company’s SPEAR T-cell therapy targeting AFP; and personnel expenses for an increased number of employees engaged in R&D.
- General and administrative (“G&A”) expenses: G&A expenses were $5.9 million for the three months ended March 31, 2016 compared to $2.4 million for the three months ended March 31, 2015. The increase was primarily due to increased personnel costs, increased share-based payment expenses, increased property costs and other costs associated with being a public company.
- Net loss: Net loss attributable to holders of the Company’s ordinary shares was $15.6 million for the three months ended March 31, 2016. This equates to $(0.04) per ordinary share or $(0.22) per American Depositary Share.
The Company will not hold a conference call to discuss these results having provided a full update during its 2016 Investor and Analyst Day held on April 22, 2016. A replay of the webcast from the event will be available on the Company’s website for 30 days following the event at ir.adaptimmune.com
Adaptimmune is reiterating its cash burn guidance. For the full year 2016, the Company expects its cash burn to be between $80 and $100 million and expects its total liquidity position at December 31, 2016, including cash, cash equivalents and short term deposits, to be at least $150 million. This guidance excludes any cash burn associated with potential new business development activities.
As previously announced, in order to align more closely with many of its peer group of biotechnology companies, the Company has changed its fiscal year to a calendar year and is reporting its financial results in U.S. dollars under U.S. GAAP, effective from January 2016. Further information on these changes is set forth below under ‘Initial Adoption of U.S. GAAP’. The Company’s next fiscal year end will be December 31, 2016.
Adaptimmune is a clinical stage biopharmaceutical company focused on novel cancer immunotherapy products based on its SPEAR™ (Specific Peptide Enhanced Affinity Receptor) T-cell platform. Established in 2008, the company aims to utilize the body’s own machinery - the T-cell - to target and destroy cancer cells by using engineered, increased affinity TCRs as a means of strengthening natural patient T-cell responses. Adaptimmune’s lead program is a SPEAR T-cell therapy targeting the NY-ESO cancer antigen. Its NY-ESO SPEAR T-cell therapy has demonstrated signs of efficacy and tolerability in Phase 1/2 trials in solid tumors and in hematologic cancer types, including synovial sarcoma and multiple myeloma. Adaptimmune has a strategic collaboration and licensing agreement with GlaxoSmithKline for the development and commercialization of the NY-ESO TCR program. In addition, Adaptimmune has a number of proprietary programs. The company has identified over 30 intracellular target peptides preferentially expressed in cancer cells and is currently progressing 12 through unpartnered research programs. Adaptimmune has over 200 employees and is located in Oxfordshire, U.K. and Philadelphia, USA. For more information: http://www.adaptimmune.com
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 Annual Report on Form 20-F filed with the Securities and Exchange Commission (SEC) on October 13, 2015, and our other SEC filings. The forward-looking statements contained in this press release speak only as of the date the statements were made and we do not undertake any obligation to update such forward-looking statements to reflect subsequent events or circumstances.
Total Liquidity Position (a non-GAAP financial measure)
Total liquidity position (a non-GAAP financial measure) is defined as cash and cash equivalents plus short-term deposits. Each of these components appears in the Consolidated Statements of Financial Position. The U.S. GAAP financial measure most directly comparable to total liquidity position is cash and cash equivalents as reported in the Consolidated Financial Statements.
We believe that the presentation of total liquidity position provides useful information to investors because management reviews total liquidity position as part of its management of overall liquidity, financial flexibility, capital structure and leverage.
|Condensed Consolidated Statement of Operations||Three months ended March 31,|
|(unaudited, in thousands, except per share data)||2016||2015|
|Research and development||(13,888||)||(5,976||)|
|General and administrative||(5,855||)||(2,359||)|
|Total operating expenses||(19,743||)||(8,335||)|
|Other income, net||1,049||3,603|
|Total other income, net||1,308||3,713|
|Loss before income taxes||$||(15,517||)||$||(1,894||)|
|Deemed dividend on convertible preferred shares||-||(6,434||)|
|Net loss available to ordinary shareholders||$||(15,576||)||$||(8,379||)|
|Net loss per ordinary share, basic and diluted (2)||$||(0.04||)||$||(0.05||)|
|Weighted average ordinary shares outstanding,|
|Basic and diluted||424,711,900||181,370,100|
|(2) The effects of the following potentially dilutive equity instruments have been excluded from the diluted loss per share calculation because they would have an antidilutive effect on the loss per share for the period|
|Three months ended March 31,|
|Condensed Consolidated Balance Sheets||March 31,||December 31,|
|(unaudited, in thousands)||2016||2015|
|Cash and cash equivalents||$||163,766||$||194,263|
|Accounts receivable, net of allowance for doubtful accounts of $- and $-||1||744|
|Other current assets and prepaid expenses (including current portion of clinical materials)||12,457||13,420|
|Total current assets||$||238,561||$||263,047|
|Property, plant & equipment, net||13,845||13,225|
|Liabilities and Stockholders’ equity|
|Accrued expenses and other accrued liabilities||5,321||7,518|
|Total current liabilities||19,838||27,889|
|Deferred revenue, less current portion||22,776||22,939|
|Common stock - Ordinary shares par value £0.001, 574.7 million authorized and 424,711,900 issued and outstanding (2015: 574.7 million authorized and 424,711,900 issued and outstanding)||682||682|
|Additional paid in capital||334,258||332,184|
|Accumulated other comprehensive loss||(10,684||)||(8,139||)|
|Total liabilities and stockholders’ equity||$||261,560||$||285,821|
|Condensed Consolidated Cash Flow Statement||Three months ended March 31,|
|(unaudited, in thousands)||2016||2015|
|Cash flows from operating activities|
|Share-based compensation expense||2,074||1,482|
|Unrealized foreign exchange gains||(1,608||)||(3,604||)|
|Changes in operating assets and liabilities:|
|(Decrease)/increase in receivables and other operating assets||(489||
|Decrease in non-current operating assets||1,835||-|
|Decrease in payables and deferred revenue||(5,660||
|Net cash used in operating activities||(18,679||)||(5,643||)|
|Cash flows from investing activities|
|Acquisition of property, plant & equipment||(1,708||)||(672||)|
|Acquisition of intangibles||(861||)||-|
|Maturity of short-term deposits||7,993||-|
|Investment in short-term deposits||(15,988||)||-|
|Net cash used in investing activities||(10,564||)||(672||)|
|Cash flows from financing activities|
|Net cash used in financing activities||-||-|
|Effect of currency exchange rate changes on cash and cash equivalents||(1,254||)||(2,750||)|
|Net decrease in cash and cash equivalents||(30,497||)||(9,065||)|
|Cash and cash equivalents at start of period||194,263||101,664|
|Cash and cash equivalents at end of period||$||163,766||$||92,599|
Initial adoption of U.S.GAAP
The Company is reporting under U.S. GAAP in U.S. dollars from January 1, 2016. The Company has previously prepared financial statements in accordance with International Financial Reporting Standards (IFRS) in pounds sterling. For the purpose of analyzing comparative periods, the Company has provided the quarterly income statement (unaudited) and the Total Liquidity Position (a non-GAAP measure) for the four quarters of the 2015 calendar year under U.S. GAAP below (in thousands):
|(unaudited, in thousands, except per share data)||March 31, 2015||June 30, 2015||September 30, 2015||December 31, 2015|
|Research and development||(5,976||)||(8,404||)||(8,276||)||(15,968||)|
|General and administrative||(2,359||)||(5,486||)||(4,979||)||(6,166||)|
|Total operating expenses||(8,335||)||(13,890||)||(13,255||)||(22,134||)|
|Other income/(expense), net||3,603||(3,502||)||1,851||1,015|
|Total other income/(expense), net||3,713||(3,314||)||2,086||1,269|
|Loss before taxes||(1,894||)||(14,421||)||(6,221||)||(16,834||)|
|Deemed dividend on Preferred Shares||(6,434||)||(2,229||)||-||-|
|Net loss available to ordinary shareholders||$||(8,379||)||$||(16,797||)||$||(6,241||)||$||(16,759||)|
Net loss per ordinary share, basic and diluted
|Cash and cash equivalents||$||92,599||$||229,046||$||217,218||$||194,263|
|Total liquidity position||$||117,179||$||284,338||$||272,091||$||248,883|
1 Total liquidity position is a non GAAP financial measure, which is explained and reconciled to the most directly comparable financial measures prepared in accordance with GAAP below.
Adaptimmune Contacts: Will Roberts Vice President, Investor Relations T: (215) 825-9306 E: email@example.com Margaret Henry Head of PR T: +44 (0)1235 430036 Mobile: +44 (0)7710 304249 E: firstname.lastname@example.org
Released May 12, 2016