-- Net cash used in operating and investing activities was $36.3 million in
the second quarter and $76.5 million for the first six months of 2017;
quarter-end cash and restricted cash position of $475.8 million, provides
funding to advance diverse pipeline
-- Initiated, with Roche, the global Phase 2 PASADENA study of PRX002/RG7935
in patients with early Parkinson's disease, triggering a $30 million
milestone payment from Roche to Prothena
-- Completed enrollment in the Phase 3 VITAL Amyloidosis Study evaluating
NEOD001 in newly diagnosed, treatment naïve patients with AL amyloidosis
and cardiac dysfunction
-- Strengthened management team with appointments of Sarah Noonberg, MD, PhD
as Chief Medical Officer and Wagner Zago, PhD as Chief Scientific Officer
DUBLIN, Ireland, Aug. 08, 2017 (GLOBE NEWSWIRE) -- Prothena Corporation plc (NASDAQ:PRTA), a late-stage clinical biotechnology company focused on the discovery, development and commercialization of novel protein immunotherapies, today reported financial results for the second quarter and first six months of 2017. In addition, the Company provided an update on its R&D programs.
"During the quarter, we achieved two important milestones in our first-in-class protein immunotherapy pipeline, completing enrollment of our Phase 3 VITAL Amyloidosis Study evaluating NEOD001 in newly diagnosed, treatment naïve patients with AL amyloidosis and cardiac dysfunction, and initiating the Phase 2 PASADENA study of PRX002/RG7935 in patients with early Parkinson's disease," said Gene Kinney, PhD, President and Chief Executive Officer of Prothena. "We also appointed two exceptionally talented leaders into key roles to further expand our ability to advance our R&D pipeline. Looking ahead, we expect topline results from our Phase 1b MAD study of PRX003 in patients with psoriasis in October, and topline results from our Phase 2b PRONTO study of NEOD001 in patients with AL amyloidosis in the second quarter of 2018. With both the PRONTO and VITAL studies now fully enrolled, our team is focused on activities to support registration submissions for NEOD001."
Second Quarter 2017 and Recent Highlights:
-- Initiated the Phase 2 PASADENA study of PRX002/RG7935 in patients with early Parkinson's disease, triggering a $30 million milestone payment from Roche to Prothena. PASADENA is a global two-part clinical study that is being conducted by Roche. The primary endpoint of this study is the comparison of change from baseline in the Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDS-UPDRS) total score (parts 1, 2 and 3) at week 52 in each of the two treatment groups vs. the placebo group. -- Completed enrollment in the Phase 3 VITAL Amyloidosis Study evaluating NEOD001 in newly diagnosed, treatment naïve patients with AL amyloidosis and cardiac dysfunction. The original target enrollment of 236 patients was exceeded and 260 patients have been randomized into the study. The VITAL study is a global, double-blind, placebo-controlled, registrational study with an event-based composite primary endpoint of all-cause mortality or cardiac hospitalizations as qualifying events. Secondary endpoints include biomarker, quality of life and functional measures. -- In a late-breaking therapeutic strategies session at the 13th ?International Conference on Alzheimer's and Parkinson's Diseases (AD/PD), Dr. Joseph Jankovic of Baylor College of Medicine presented clinical data from the 80-patient Phase 1b multiple ascending dose study of PRX002/RG7935 in patients with Parkinson's disease. The positive results supported advancing PRX002/RG7935 into a Phase 2 study, PASADENA. -- Appointed Sarah Noonberg, MD, PhD as Chief Medical Officer to define and advance Prothena's product pipeline and lead its clinical and medical organizations. Dr. Noonberg has extensive drug development experience across several therapeutic categories and has led large, global organizations across several phases of drug development. -- Appointed Wagner Zago, PhD as Chief Scientific Officer to define and execute Prothena's research strategy and advance its drug discovery pipeline. Dr. Zago had been Prothena's Head of Research since 2015 and has led teams that have advanced four programs based on novel mechanisms into clinical development.
Upcoming Research and Development Milestones
NEOD001 is a monoclonal antibody for the potential treatment of AL amyloidosis:
-- Topline results in the Phase 2b PRONTO study (129 patients) expected in the second quarter of 2018
PRX003 is a monoclonal antibody for the potential treatment of inflammatory diseases, including psoriasis and psoriatic arthritis:
-- Topline results from the Phase 1b multiple ascending dose, safety and proof-of-biology study in 32 patients (8 patients per dose-level cohort, randomized 3:1) with psoriasis expected in October 2017
PRX004 is a monoclonal antibody for the potential treatment of ATTR amyloidosis:
-- Clinical development expected to begin by mid-2018
Second Quarter and First Six Months of 2017 Financial Results
Prothena reported a net loss of $17.7 million and $53.1 million for the second quarter and first six months of 2017, respectively, as compared to a net loss of $40.4 million and $68.0 million for the second quarter and first six months of 2016, respectively. Net loss per share for the second quarter and first six months of 2017 was $0.46 and $1.44, respectively, as compared to a net loss per share of $1.18 and $1.99 for the second quarter and first six months of 2016, respectively.
Prothena reported total revenue of $26.8 million and $27.1 million for the second quarter and first six months of 2017, respectively, as compared to total revenue of $0.3 million and $0.6 million for the second quarter and first six months of 2016, respectively. The increase in revenue for the second quarter and first six months of 2017 was primarily due to achievement of a clinical milestone from Roche of $30.0 million (of which $26.6 million was recognized as collaboration revenue and $3.4 million was recognized as an offset to R&D expenses).
Research and development (R&D) expenses totaled $34.0 million and $59.7 million for the second quarter and first six months of 2017, respectively, as compared to $32.4 million and $52.9 million for the second quarter and first six months of 2016, respectively. The increase in R&D expenses for the second quarter and first six months of 2017 was primarily due to higher clinical trial and personnel cost offset in part by lower external expenses for product manufacturing. R&D expenses included non-cash share-based compensation expense of $2.7 million and $5.0 million for the second quarter and first six months of 2017, respectively, as compared to $1.8 million and $3.2 million for the second quarter and first six months of 2016, respectively.
General and administrative (G&A) expenses totaled $10.9 million and $21.7 million for the second quarter and first six months of 2017, respectively, as compared to $8.1 million and $15.3 million for second quarter and first six months of 2016, respectively. The increase in G&A expenses for the second quarter was primarily due to increases in personnel costs. The increase in G&A expenses for the first six months was primarily due to increases in personnel, consulting and other expenses partially offset by a gain recognized in the first quarter of 2017 from the assignment of our former South San Francisco facility lease. G&A expenses included non-cash share-based compensation expense of $3.9 million and $7.2 million in the second quarter and first six months of 2017, respectively, as compared to $2.7 million and $5.0 million in the second quarter and first six months of 2016, respectively.
Total non-cash share-based compensation expense was $6.7 million and $12.3 million for the second quarter and first six months of 2017, respectively, as compared to $4.5 million and $8.3 million for the second quarter and first six months of 2016, respectively.
As of June 30, 2017, Prothena had $475.8 million in cash, cash equivalents and restricted cash and no debt.
As of July 21, 2017, Prothena had approximately 38.3 million ordinary shares outstanding.
The Company expects the full year 2017 net cash burn from operating and investing activities to be $160 to $170 million, which includes the milestone from Roche earned in the second quarter of 2017 upon initiation of the Phase 2 study of PRX002/RG7935, and to end the year with approximately $375 million in cash, cash equivalents and restricted cash (mid-point). The estimated full year 2017 net cash burn from operating and investing activities is primarily driven by an estimated net loss of $177 to $191 million, which includes an estimated $26 million of non-cash share-based compensation expense.
About Prothena
Prothena Corporation plc is a global, late-stage clinical biotechnology company establishing fully-integrated research, development and commercial capabilities. Fueled by its deep scientific understanding built over decades of research in protein misfolding and cell adhesion - the root causes of many serious or currently untreatable amyloid and inflammatory diseases - Prothena seeks to fundamentally change the course of progressive diseases associated with this biology. The Company's pipeline of antibody therapeutic candidates targets a number of indications including AL amyloidosis (NEOD001), Parkinson's disease and other related synucleinopathies (PRX002/RG7935), inflammatory diseases, including psoriasis and psoriatic arthritis (PRX003), and ATTR amyloidosis (PRX004). The Company continues discovery of additional novel therapeutic candidates where its deep scientific understanding of disease pathology can be leveraged. For more information, please visit the Company's website at www.prothena.com
Forward-looking Statements
This press release contains forward-looking statements. These statements relate to, among other things, the sufficiency of our funding to advance our diverse pipeline; the timing of announcing topline results from the Phase 2b study of NEOD001; the timing of announcing topline results from the Phase 1b study of PRX003; the timing of initiating clinical development of PRX004; our expected net cash burn from operating and investing activities for 2017 and cash balance at the end of 2017; and our estimated net loss and non-cash share-based compensation expense for 2017. These statements are based on estimates, projections and assumptions that may prove not to be accurate, and actual results could differ materially from those anticipated due to known and unknown risks, uncertainties and other factors, including but not limited to the risks, uncertainties and other factors described in the "Risk Factors" sections of our Annual Report on Form 10-K filed with the Securities and Exchange Commission (SEC) on February 27, 2017 and our subsequent Quarterly Reports on Form 10-Q filed with the SEC. Prothena undertakes no obligation to update publicly any forward-looking statements contained in this press release as a result of new information, future events or changes in Prothena's expectations.
PROTHENA CORPORATION PLC CONSOLIDATED STATEMENTS OF OPERATIONS (unaudited - amounts in thousands except per share data)
Three Months Ended Six Months Ended June 30, June 30, 2017 2016 2017 2016 Collaboration revenue $ 26,812 $ 333 $ 27,071 $ 598 Total revenue 26,812 333 27,071 598 Operating expenses: Research and 34,032 32,359 59,730 52,852 development General and 10,912 8,134 21,744 15,316 administrative Total operating 44,944 40,493 81,474 68,168 expenses Loss from operations (18,132 ) (40,160 ) (54,403 ) (67,570 ) Other expense, net (856 ) (96 ) (1,630 ) (26 ) Loss before income taxes (18,988 ) (40,256 ) (56,033 ) (67,596 ) Provision for (benefit (1,287 ) 189 (2,948 ) 370 from) income taxes Net loss $ (17,70 ) $ (40,44 ) $ (53,08 ) $ (67,96 ) 1 5 5 6 Basic and diluted net $ (0.46 ) $ (1.18 ) $ (1.44 ) $ (1.99 ) loss per share Shares used to compute 38,073 34,358 36,922 34,192 basic and diluted net loss per share
PROTHENA CORPORATION PLC CONSOLIDATED BALANCE SHEETS (unaudited - amounts in thousands)
June 30, December 31, 2017 2016 Assets Cash and cash equivalents $ 471,729 $ 386,923 Other current assets 39,991 4,439 Total current assets 511,720 391,362 Property and equipment, net 55,843 56,452 Restricted cash 4,056 4,056 Other assets 7,381 8,106 Total non-current assets 67,280 68,614 Total assets $ 579,000 $ 459,976 Liabilities and Shareholders' Equity Accrued research and development $ 20,799 $ 19,073 Other current liabilities 18,800 22,002 Total current liabilities 39,599 41,075 Non-current liabilities: 52,425 53,498 Total liabilities 92,024 94,573 Total shareholders' equity 486,976 365,403 Total liabilities and shareholders' equity $ 579,000 $ 459,976
Media & Investor Contact: Ellen Rose, Head of Communications 650-922-2405, ellen.rose@prothena.com
DUBLIN, Ireland, Aug. 08, 2017 (GLOBE NEWSWIRE) -- Prothena Corporation plc (NASDAQ:PRTA), a late-stage clinical biotechnology company focused on the discovery, development and commercialization of novel protein immunotherapies, today reported financial results for the second quarter and first six months of 2017. In addition, the Company provided an update on its R&D programs.
"During the quarter, we achieved two important milestones in our first-in-class protein immunotherapy pipeline, completing enrollment of our Phase 3 VITAL Amyloidosis Study evaluating NEOD001 in newly diagnosed, treatment naïve patients with AL amyloidosis and cardiac dysfunction, and initiating the Phase 2 PASADENA study of PRX002/RG7935 in patients with early Parkinson's disease," said Gene Kinney, PhD, President and Chief Executive Officer of Prothena. "We also appointed two exceptionally talented leaders into key roles to further expand our ability to advance our R&D pipeline. Looking ahead, we expect topline results from our Phase 1b MAD study of PRX003 in patients with psoriasis in October, and topline results from our Phase 2b PRONTO study of NEOD001 in patients with AL amyloidosis in the second quarter of 2018. With both the PRONTO and VITAL studies now fully enrolled, our team is focused on activities to support registration submissions for NEOD001."
Second Quarter 2017 and Recent Highlights:
-- Initiated the Phase 2 PASADENA study of PRX002/RG7935 in patients with early Parkinson's disease, triggering a $30 million milestone payment from Roche to Prothena. PASADENA is a global two-part clinical study that is being conducted by Roche. The primary endpoint of this study is the comparison of change from baseline in the Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDS-UPDRS) total score (parts 1, 2 and 3) at week 52 in each of the two treatment groups vs. the placebo group. -- Completed enrollment in the Phase 3 VITAL Amyloidosis Study evaluating NEOD001 in newly diagnosed, treatment naïve patients with AL amyloidosis and cardiac dysfunction. The original target enrollment of 236 patients was exceeded and 260 patients have been randomized into the study. The VITAL study is a global, double-blind, placebo-controlled, registrational study with an event-based composite primary endpoint of all-cause mortality or cardiac hospitalizations as qualifying events. Secondary endpoints include biomarker, quality of life and functional measures. -- In a late-breaking therapeutic strategies session at the 13th ?International Conference on Alzheimer's and Parkinson's Diseases (AD/PD), Dr. Joseph Jankovic of Baylor College of Medicine presented clinical data from the 80-patient Phase 1b multiple ascending dose study of PRX002/RG7935 in patients with Parkinson's disease. The positive results supported advancing PRX002/RG7935 into a Phase 2 study, PASADENA. -- Appointed Sarah Noonberg, MD, PhD as Chief Medical Officer to define and advance Prothena's product pipeline and lead its clinical and medical organizations. Dr. Noonberg has extensive drug development experience across several therapeutic categories and has led large, global organizations across several phases of drug development. -- Appointed Wagner Zago, PhD as Chief Scientific Officer to define and execute Prothena's research strategy and advance its drug discovery pipeline. Dr. Zago had been Prothena's Head of Research since 2015 and has led teams that have advanced four programs based on novel mechanisms into clinical development.
Upcoming Research and Development Milestones
NEOD001 is a monoclonal antibody for the potential treatment of AL amyloidosis:
-- Topline results in the Phase 2b PRONTO study (129 patients) expected in the second quarter of 2018
PRX003 is a monoclonal antibody for the potential treatment of inflammatory diseases, including psoriasis and psoriatic arthritis:
-- Topline results from the Phase 1b multiple ascending dose, safety and proof-of-biology study in 32 patients (8 patients per dose-level cohort, randomized 3:1) with psoriasis expected in October 2017
PRX004 is a monoclonal antibody for the potential treatment of ATTR amyloidosis:
-- Clinical development expected to begin by mid-2018
Second Quarter and First Six Months of 2017 Financial Results
Prothena reported a net loss of $17.7 million and $53.1 million for the second quarter and first six months of 2017, respectively, as compared to a net loss of $40.4 million and $68.0 million for the second quarter and first six months of 2016, respectively. Net loss per share for the second quarter and first six months of 2017 was $0.46 and $1.44, respectively, as compared to a net loss per share of $1.18 and $1.99 for the second quarter and first six months of 2016, respectively.
Prothena reported total revenue of $26.8 million and $27.1 million for the second quarter and first six months of 2017, respectively, as compared to total revenue of $0.3 million and $0.6 million for the second quarter and first six months of 2016, respectively. The increase in revenue for the second quarter and first six months of 2017 was primarily due to achievement of a clinical milestone from Roche of $30.0 million (of which $26.6 million was recognized as collaboration revenue and $3.4 million was recognized as an offset to R&D expenses).
Research and development (R&D) expenses totaled $34.0 million and $59.7 million for the second quarter and first six months of 2017, respectively, as compared to $32.4 million and $52.9 million for the second quarter and first six months of 2016, respectively. The increase in R&D expenses for the second quarter and first six months of 2017 was primarily due to higher clinical trial and personnel cost offset in part by lower external expenses for product manufacturing. R&D expenses included non-cash share-based compensation expense of $2.7 million and $5.0 million for the second quarter and first six months of 2017, respectively, as compared to $1.8 million and $3.2 million for the second quarter and first six months of 2016, respectively.
General and administrative (G&A) expenses totaled $10.9 million and $21.7 million for the second quarter and first six months of 2017, respectively, as compared to $8.1 million and $15.3 million for second quarter and first six months of 2016, respectively. The increase in G&A expenses for the second quarter was primarily due to increases in personnel costs. The increase in G&A expenses for the first six months was primarily due to increases in personnel, consulting and other expenses partially offset by a gain recognized in the first quarter of 2017 from the assignment of our former South San Francisco facility lease. G&A expenses included non-cash share-based compensation expense of $3.9 million and $7.2 million in the second quarter and first six months of 2017, respectively, as compared to $2.7 million and $5.0 million in the second quarter and first six months of 2016, respectively.
Total non-cash share-based compensation expense was $6.7 million and $12.3 million for the second quarter and first six months of 2017, respectively, as compared to $4.5 million and $8.3 million for the second quarter and first six months of 2016, respectively.
As of June 30, 2017, Prothena had $475.8 million in cash, cash equivalents and restricted cash and no debt.
As of July 21, 2017, Prothena had approximately 38.3 million ordinary shares outstanding.
The Company expects the full year 2017 net cash burn from operating and investing activities to be $160 to $170 million, which includes the milestone from Roche earned in the second quarter of 2017 upon initiation of the Phase 2 study of PRX002/RG7935, and to end the year with approximately $375 million in cash, cash equivalents and restricted cash (mid-point). The estimated full year 2017 net cash burn from operating and investing activities is primarily driven by an estimated net loss of $177 to $191 million, which includes an estimated $26 million of non-cash share-based compensation expense.
About Prothena
Prothena Corporation plc is a global, late-stage clinical biotechnology company establishing fully-integrated research, development and commercial capabilities. Fueled by its deep scientific understanding built over decades of research in protein misfolding and cell adhesion - the root causes of many serious or currently untreatable amyloid and inflammatory diseases - Prothena seeks to fundamentally change the course of progressive diseases associated with this biology. The Company's pipeline of antibody therapeutic candidates targets a number of indications including AL amyloidosis (NEOD001), Parkinson's disease and other related synucleinopathies (PRX002/RG7935), inflammatory diseases, including psoriasis and psoriatic arthritis (PRX003), and ATTR amyloidosis (PRX004). The Company continues discovery of additional novel therapeutic candidates where its deep scientific understanding of disease pathology can be leveraged. For more information, please visit the Company's website at www.prothena.com
Forward-looking Statements
This press release contains forward-looking statements. These statements relate to, among other things, the sufficiency of our funding to advance our diverse pipeline; the timing of announcing topline results from the Phase 2b study of NEOD001; the timing of announcing topline results from the Phase 1b study of PRX003; the timing of initiating clinical development of PRX004; our expected net cash burn from operating and investing activities for 2017 and cash balance at the end of 2017; and our estimated net loss and non-cash share-based compensation expense for 2017. These statements are based on estimates, projections and assumptions that may prove not to be accurate, and actual results could differ materially from those anticipated due to known and unknown risks, uncertainties and other factors, including but not limited to the risks, uncertainties and other factors described in the "Risk Factors" sections of our Annual Report on Form 10-K filed with the Securities and Exchange Commission (SEC) on February 27, 2017 and our subsequent Quarterly Reports on Form 10-Q filed with the SEC. Prothena undertakes no obligation to update publicly any forward-looking statements contained in this press release as a result of new information, future events or changes in Prothena's expectations.
PROTHENA CORPORATION PLC CONSOLIDATED STATEMENTS OF OPERATIONS (unaudited - amounts in thousands except per share data)
Three Months Ended Six Months Ended June 30, June 30, 2017 2016 2017 2016 Collaboration revenue $ 26,812 $ 333 $ 27,071 $ 598 Total revenue 26,812 333 27,071 598 Operating expenses: Research and 34,032 32,359 59,730 52,852 development General and 10,912 8,134 21,744 15,316 administrative Total operating 44,944 40,493 81,474 68,168 expenses Loss from operations (18,132 ) (40,160 ) (54,403 ) (67,570 ) Other expense, net (856 ) (96 ) (1,630 ) (26 ) Loss before income taxes (18,988 ) (40,256 ) (56,033 ) (67,596 ) Provision for (benefit (1,287 ) 189 (2,948 ) 370 from) income taxes Net loss $ (17,70 ) $ (40,44 ) $ (53,08 ) $ (67,96 ) 1 5 5 6 Basic and diluted net $ (0.46 ) $ (1.18 ) $ (1.44 ) $ (1.99 ) loss per share Shares used to compute 38,073 34,358 36,922 34,192 basic and diluted net loss per share
PROTHENA CORPORATION PLC CONSOLIDATED BALANCE SHEETS (unaudited - amounts in thousands)
June 30, December 31, 2017 2016 Assets Cash and cash equivalents $ 471,729 $ 386,923 Other current assets 39,991 4,439 Total current assets 511,720 391,362 Property and equipment, net 55,843 56,452 Restricted cash 4,056 4,056 Other assets 7,381 8,106 Total non-current assets 67,280 68,614 Total assets $ 579,000 $ 459,976 Liabilities and Shareholders' Equity Accrued research and development $ 20,799 $ 19,073 Other current liabilities 18,800 22,002 Total current liabilities 39,599 41,075 Non-current liabilities: 52,425 53,498 Total liabilities 92,024 94,573 Total shareholders' equity 486,976 365,403 Total liabilities and shareholders' equity $ 579,000 $ 459,976
Media & Investor Contact: Ellen Rose, Head of Communications 650-922-2405, ellen.rose@prothena.com