Spark Therapeutics Reports Third Quarter 2015 Financial Results And Recent Business Highlights
Reported positive top-line results from pivotal Phase 3 trial of SPK-RPE65 for genetic blinding conditions
Durability of effect of SPK-RPE65 reported at three years with observation ongoing
Continued progression and expansion of pipeline and operations
PHILADELPHIA, Nov. 04, 2015 (GLOBE NEWSWIRE) -- Spark Therapeutics (NASDAQ:ONCE) today announced financial results for the quarter ended September 30, 2015 and updated investors on its operational progress.
“Last month we released positive Phase 3 data from the pivotal trial of our lead program, SPK-RPE65, for the treatment of genetic blinding conditions. The results marked an important milestone for Spark and great news for patients suffering from RPE65-mediated inherited retinal dystrophies, that are now one step closer to having a potential treatment,” said Jeffrey D. Marrazzo, co-founder and chief executive officer of Spark. “This trial was the first randomized controlled Phase 3 trial of a gene therapy for a genetic disease, and the results further validate Spark’s platform which is being applied across a growing pipeline of clinical and preclinical gene therapy programs,” added Mr. Marrazzo.
Recent highlights:
• Reported Positive Top-line Results from Pivotal Phase 3 Trial of SPK-RPE65: The pivotal Phase 3 trial met its primary endpoint, the bilateral mobility test (MT) change score (p = .001), and the first two of three secondary endpoints: full-field light sensitivity threshold testing (p < .001) and first eye MT change score (p =.001). There were no serious adverse events related to SPK-RPE65 or deleterious immune responses observed in the trial. In the trial, SPK-RPE65 demonstrated the ability to substantially restore vision, with thirteen of the 20 subjects receiving SPK-RPE65 achieving the maximum improvement measurable on the mobility test, and with the intervention group improving approximately 100-fold in light sensitivity on average.
• SPK-RPE65 Continues to Demonstrate Long-lasting Effect: At the Retina Society 48th Annual Scientific Meeting in Paris, principal investigator Dr. Stephen R. Russell presented data demonstrating the continued durability of the improvements seen in a cohort of subjects from an earlier Phase 1 trial, as measured by mobility testing and FST. This cohort of subjects (n = 8), that would have met the Phase 3 eligibility criteria and that received the same dose of SPK-RPE65 that was administered in the Phase 3 trial, is now out three years, with measurements ongoing.
• Clinical Programs Continue to Make Operational Progress: Spark’s two additional clinical-stage programs continue to advance: the Phase 1/2 trial of SPK-CHM for choroideremia is now enrolling subjects in the second dose cohort, with no reported product-related serious adverse events, and the Phase 1/2 clinical trial for the SPK-FIX program for hemophilia B, in collaboration with Pfizer, is open for enrollment.
• Expanded Human Capital and Strong Financial Position: We continue to grow our team across all disciplines, with the number of employees having doubled so far in 2015 to nearly 100. The balance sheet remains strong, with over $212.2 million in cash and cash equivalents at September 30, 2015.
Financial Results
Three Months Ended September 30, 2014 and 2015
In the three months ended September 30, 2015, we recognized $1.3 million of revenue associated with our Pfizer collaboration as compared to zero in the three months ended September 30, 2014.
Our research and development expenses for the three months ended September 30, 2015 were $11.8 million versus $4.7 million for the three months ended September 30, 2014. The $7.1 million increase was due to a $5.2 million increase in internal research and development expenses, primarily due to significantly increased headcount, and an increase of $1.9 million in external research and development, primarily from an increase of $1.3 million in expenses related to clinical trials for SPK-RP65, SPK-CHM, and SPK-FIX and $0.7 million related to other product candidates.
General and administrative expenses for the three months ended September 30, 2015 were $6.5 million versus $2.1 million for the three months ended September 30, 2014. General and administrative expenses consisted primarily of salaries and related costs, including stock-based compensation, legal and patent costs and other professional fees. The $4.4 million increase primarily was due to increased headcount, including stock-based compensation, and costs associated with operating as a public company.
Our net loss applicable to common stockholders for the three months ended September 30, 2015 was $16.9 million, or ($0.70) basic and diluted net loss per common share, as compared with a net loss applicable to common stockholders of $6.8 million, or ($1.22) basic and diluted net loss per common share for the three months ended September 30, 2014. Nine Months Ended September 30, 2014 and 2015
In the nine months ended September 30, 2015, we recognized $3.9 million of revenue associated with our Pfizer collaboration and $1.0 million of a non-refundable payment after we concluded discussions on a potential agreement with a pharmaceutical company. In the nine months ended September 30, 2014, we recognized $20,000 of revenue associated with our Genable agreement.
Our research and development expenses for the nine months ended September 30, 2015 were $29.5 million versus $10.2 million for the nine months ended September 30, 2014. The $19.3 million increase was due to a $16.0 million increase in internal research and development expenses, primarily due to significantly increased headcount, and an increase of $3.3 million in external research and development, primarily from an increase of $1.8 million in expenses related to clinical trials for SPK-CHM and SPK-FIX as well as an increase of $1.5 million in other product candidates.
General and administrative expenses for the nine months ended September 30, 2015 were $16.5 million versus $5.2 million for the nine months ended September 30, 2014. General and administrative expenses consisted primarily of salaries and related costs, including stock-based compensation, legal and patent costs and other professional fees. The $11.3 million increase was primarily due to increased headcount, including stock-based compensation, and costs associated with operating as a public company.
Our net loss applicable to common stockholders for the nine months ended September 30, 2015 was $41.6 million, or ($1.88) basic and diluted net loss per common share, as compared with a net loss applicable to common stockholders of $15.3 million, or ($2.87) basic and diluted net loss per common share for the nine months ended September 30, 2014.
As of September 30, 2015, Spark had cash and cash equivalents of $212.2 million, with 24.6 million shares outstanding.
About Spark Therapeutics
Spark is a gene therapy leader seeking to transform the lives of patients suffering from debilitating genetic diseases by developing one-time, life-altering treatments. Spark’s initial focus is on treating rare diseases where no, or only palliative, therapies exist. Spark’s most advanced product candidate, SPK-RPE65, which has received both breakthrough therapy and orphan product designation, recently reported positive top-line results from a pivotal Phase 3 clinical trial for the treatment of rare blinding conditions. Spark’s validated gene therapy platform is being applied to a range of clinical and preclinical programs addressing serious genetic diseases, including inherited retinal dystrophies, hematologic disorders and neurodegenerative diseases. Spark builds on two decades of research, development and manufacturing at The Children’s Hospital of Philadelphia, including human trials conducted across diverse therapeutic areas and routes of administration. To learn more, please visit www.sparktx.com.
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Durability of effect of SPK-RPE65 reported at three years with observation ongoing
Continued progression and expansion of pipeline and operations
PHILADELPHIA, Nov. 04, 2015 (GLOBE NEWSWIRE) -- Spark Therapeutics (NASDAQ:ONCE) today announced financial results for the quarter ended September 30, 2015 and updated investors on its operational progress.
“Last month we released positive Phase 3 data from the pivotal trial of our lead program, SPK-RPE65, for the treatment of genetic blinding conditions. The results marked an important milestone for Spark and great news for patients suffering from RPE65-mediated inherited retinal dystrophies, that are now one step closer to having a potential treatment,” said Jeffrey D. Marrazzo, co-founder and chief executive officer of Spark. “This trial was the first randomized controlled Phase 3 trial of a gene therapy for a genetic disease, and the results further validate Spark’s platform which is being applied across a growing pipeline of clinical and preclinical gene therapy programs,” added Mr. Marrazzo.
Recent highlights:
• Reported Positive Top-line Results from Pivotal Phase 3 Trial of SPK-RPE65: The pivotal Phase 3 trial met its primary endpoint, the bilateral mobility test (MT) change score (p = .001), and the first two of three secondary endpoints: full-field light sensitivity threshold testing (p < .001) and first eye MT change score (p =.001). There were no serious adverse events related to SPK-RPE65 or deleterious immune responses observed in the trial. In the trial, SPK-RPE65 demonstrated the ability to substantially restore vision, with thirteen of the 20 subjects receiving SPK-RPE65 achieving the maximum improvement measurable on the mobility test, and with the intervention group improving approximately 100-fold in light sensitivity on average.
• SPK-RPE65 Continues to Demonstrate Long-lasting Effect: At the Retina Society 48th Annual Scientific Meeting in Paris, principal investigator Dr. Stephen R. Russell presented data demonstrating the continued durability of the improvements seen in a cohort of subjects from an earlier Phase 1 trial, as measured by mobility testing and FST. This cohort of subjects (n = 8), that would have met the Phase 3 eligibility criteria and that received the same dose of SPK-RPE65 that was administered in the Phase 3 trial, is now out three years, with measurements ongoing.
• Clinical Programs Continue to Make Operational Progress: Spark’s two additional clinical-stage programs continue to advance: the Phase 1/2 trial of SPK-CHM for choroideremia is now enrolling subjects in the second dose cohort, with no reported product-related serious adverse events, and the Phase 1/2 clinical trial for the SPK-FIX program for hemophilia B, in collaboration with Pfizer, is open for enrollment.
• Expanded Human Capital and Strong Financial Position: We continue to grow our team across all disciplines, with the number of employees having doubled so far in 2015 to nearly 100. The balance sheet remains strong, with over $212.2 million in cash and cash equivalents at September 30, 2015.
Financial Results
Three Months Ended September 30, 2014 and 2015
In the three months ended September 30, 2015, we recognized $1.3 million of revenue associated with our Pfizer collaboration as compared to zero in the three months ended September 30, 2014.
Our research and development expenses for the three months ended September 30, 2015 were $11.8 million versus $4.7 million for the three months ended September 30, 2014. The $7.1 million increase was due to a $5.2 million increase in internal research and development expenses, primarily due to significantly increased headcount, and an increase of $1.9 million in external research and development, primarily from an increase of $1.3 million in expenses related to clinical trials for SPK-RP65, SPK-CHM, and SPK-FIX and $0.7 million related to other product candidates.
General and administrative expenses for the three months ended September 30, 2015 were $6.5 million versus $2.1 million for the three months ended September 30, 2014. General and administrative expenses consisted primarily of salaries and related costs, including stock-based compensation, legal and patent costs and other professional fees. The $4.4 million increase primarily was due to increased headcount, including stock-based compensation, and costs associated with operating as a public company.
Our net loss applicable to common stockholders for the three months ended September 30, 2015 was $16.9 million, or ($0.70) basic and diluted net loss per common share, as compared with a net loss applicable to common stockholders of $6.8 million, or ($1.22) basic and diluted net loss per common share for the three months ended September 30, 2014. Nine Months Ended September 30, 2014 and 2015
In the nine months ended September 30, 2015, we recognized $3.9 million of revenue associated with our Pfizer collaboration and $1.0 million of a non-refundable payment after we concluded discussions on a potential agreement with a pharmaceutical company. In the nine months ended September 30, 2014, we recognized $20,000 of revenue associated with our Genable agreement.
Our research and development expenses for the nine months ended September 30, 2015 were $29.5 million versus $10.2 million for the nine months ended September 30, 2014. The $19.3 million increase was due to a $16.0 million increase in internal research and development expenses, primarily due to significantly increased headcount, and an increase of $3.3 million in external research and development, primarily from an increase of $1.8 million in expenses related to clinical trials for SPK-CHM and SPK-FIX as well as an increase of $1.5 million in other product candidates.
General and administrative expenses for the nine months ended September 30, 2015 were $16.5 million versus $5.2 million for the nine months ended September 30, 2014. General and administrative expenses consisted primarily of salaries and related costs, including stock-based compensation, legal and patent costs and other professional fees. The $11.3 million increase was primarily due to increased headcount, including stock-based compensation, and costs associated with operating as a public company.
Our net loss applicable to common stockholders for the nine months ended September 30, 2015 was $41.6 million, or ($1.88) basic and diluted net loss per common share, as compared with a net loss applicable to common stockholders of $15.3 million, or ($2.87) basic and diluted net loss per common share for the nine months ended September 30, 2014.
As of September 30, 2015, Spark had cash and cash equivalents of $212.2 million, with 24.6 million shares outstanding.
About Spark Therapeutics
Spark is a gene therapy leader seeking to transform the lives of patients suffering from debilitating genetic diseases by developing one-time, life-altering treatments. Spark’s initial focus is on treating rare diseases where no, or only palliative, therapies exist. Spark’s most advanced product candidate, SPK-RPE65, which has received both breakthrough therapy and orphan product designation, recently reported positive top-line results from a pivotal Phase 3 clinical trial for the treatment of rare blinding conditions. Spark’s validated gene therapy platform is being applied to a range of clinical and preclinical programs addressing serious genetic diseases, including inherited retinal dystrophies, hematologic disorders and neurodegenerative diseases. Spark builds on two decades of research, development and manufacturing at The Children’s Hospital of Philadelphia, including human trials conducted across diverse therapeutic areas and routes of administration. To learn more, please visit www.sparktx.com.
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