Spark Therapeutics (ONCE), focuses on the development of gene therapy products for patients suffering from debilitating genetic diseases.
ONCE’s products include voretigene neparvovec, which is in Phase III clinical trial for the treatment of genetic blinding conditions called inherited retinal diseases caused by non-sex-linked, autosomal recessive, or biallelic mutations in the RPE65 gene; and SPK-CHM that is in Phase I/II clinical trial for the treatment of choroideremia.
ONCE's products also comprise SPK-7001 that is in Phase 1/2 trial for choroideremia; SPK-9001, which is in Phase 1/2 trial for hemophilia B; and SPK-8011 that is in Phase 1/2 trial hemophilia A. In addition, its product candidates and development programs include SPK-FVIII program to treat hemophilia A; SPK-TPP1 program for the treatment of a form of Batten disease and Huntington's disease; RhoNova for the treatment of rhodopsin-linked autosomal dominant retinitis pigmentosa; and SPK-LHON for treating Leber hereditary optic neuropathy, as well as preclinical programs in development for the treatment of rare genetic blinding conditions, hematologic disorders, and other neurodegenerative diseases.
ONCE has collaboration agreement with Pfizer, Inc. for the development and commercialization of SPK-FIX product candidates in its gene therapy program for the treatment of hemophilia B.
Spark Therapeutics, Inc. was founded in 2013 and is headquartered in Philadelphia, Pennsylvania.
April 29, 2020
RegMed Investors’ (RMi) closing bell: markets moved as a treatment option, remdesivir helped patient recover more quickly
April 28, 2020
RegMed Investors’ (RMi) closing bell: yesterday’s upside strength did not sustain the sector’s share pricing today
April 22, 2020
RegMed Investors’ (RMi) pre-open: sessions alternate with positive/negative closes as indexes and markets spin the bottle
April 21, 2020
RegMed Investors’ (RMi) closing bell: they came for the upsiders, put a black bag over their heads and dragged them out
April 20, 2020
RegMed Investors’ (RMi) closing bell: sector closed positive as indexes dived
April 20, 2020
RegMed Investors’ (RMi) pre-open: the test we need for this market is for confidence
April 17, 2020
RegMed Investors’ (RMi) closing bell: sector stocks stumbled 3 times this week, then wrestled to win with a sentiment comeback
April 16, 2020
RegMed Investors’ (RMi) pre-open: there are less winners and more losers in share pricing
April 15, 2020
RegMed Investors’ (RMi) closing bell: As I had stated, yesterday’s rally will give way to renewed selling pressure
April 13, 2020
RegMed Investors’ (RMi) pre-open: it’s coming, expect a retest of the market’s March low
35 companies, 1 interpreter!
Insight, foresight and recommendation
Spark Therapeutics (ONCE) -- Opened 1/18 at $53.31, slipped to $50.56 (1/5) ending the month at $56.05 and started February at $56.30 and has been slippin, dipping and retesting lows such as 2/20's $50.23 a believer. ONCE has built a fully integrated company dedicated to discovering, developing and delivering one-time treatments that provide long-lasting, transformative outcomes to patients, families, society and the health care system. In 2018, ONCE is focused on launching LUXTURNA in the U.S. and securing marketing authorization in the EU, advancing its global development program for SPK-8011 in hemophilia A and also continuing to progress its pipeline of other investigational gene therapies. Recent: entered into an amendment to the license agreement for SPK-9001 with Pfizer (PFE), in 11/17; including an initial $10 million cash payment and up to an additional $15 million in potential milestone payments upon completion of certain transitional activities in mid-2018 and also ntered into a supply agreement with PFE in February 2018 to begin production this quarter for one batch of drug substance expected to be used for Phase 3 development; Spark received $7 million up front and will receive up to $7 million upon delivery. Dips are always due to market conditions but, with $540.2 M in cash excludes the $105 million received from Novartis in 1/18 and is eligible to receive an additional $25 million upon approval by European Medicines Agency (EMA) and total of $40 million in aggregate additional milestones on initial sales in multiple ex-U.S. markets
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