Not exact matches
Our goal is to complement the
current strategic interest
of Chiesi Farmaceutici in the space
of rare
diseases by investing in early
stage opportunities and accelerate the expansion
of the Chiesi network in the US among universities, venture capital investors, rare
disease patient organizations and start - ups developing treatments for rare
diseases.
«Unfortunately, the
current standard laboratory test is often unable to detect Lyme
disease at an early
stage of the infection,» explains Hannes Stockinger, Head
of the Institute for Hygiene and Applied Immunology
of the Center for Pathophysiology, Infectionology and Immunology
of MedUni Vienna.
Electrophysiological testing to measure peripheral nerve conduction properties is not a viable alternative because
current methods lack the sensitivity required to detect damage to small, unmyelinated fibers, especially in early
stages of disease.
In the
current study, deploying TFPI and an isoform
of tenascin C, TNC - FN IIIC, with CA 19 - 9 improved performance discriminating
stage I and II
disease from healthy or benign
disease controls.
Adding two blood - borne proteins associated with cancer cell migration increases the predictive ability
of the
current biomarker for pancreatic cancer to detect early
stage disease, a research team from The University
of Texas MD Anderson Cancer Center reports in the Journal
of the National Cancer Institute.
The
current study enrolled 161 participants — 100 with end -
stage kidney
disease, all
of whom were dialysis dependent; 36 with chronic
disease not yet at the end
stage, and 25 healthy controls.
Properly diagnosing Lyme
disease can at times be challenging because
of the limitations
of the
current laboratory test, particularly during the early
stages of disease.
The only
current treatment for end -
stage liver
disease is a liver transplant, and the number
of livers available from deceased donors is limited.
So clinical trials are certainly something that are still far away at the
current stage, but it is certainly worthwhile to follow our experimental approach both in vitro and in vivo, in order to test whether at some
stage we can really move forward and test, whether by reprogramming endogenous cells, we can reconstitute neural circuits that are damaged or deceased; and, thereby also improve the lives
of many people that suffer neurological
diseases.
Table 1: Selection, Design & Construction
of HSV - based Oncolytic Viruses Table 2: Selection, Design & Construction
of Adenovirus - based Oncolytic Viruses Table 3: Selection, Design & Construction
of Vaccinia Virus - based Oncolytic Viruses Table 4: Selection, Design & Construction
of Vesicular Stomatitis Virus - based Oncolytic Viruses Table 5: Selection, Design & Construction
of Newcastle
Disease Virus - based Oncolytic Viruses Table 6: Selection, Design & Construction
of Various Virus - based Oncolytic Viruses Table 7:
Current Company - Sponsored Clinical Trials
of T - Vec Table 8: Clinical Trials
of ColoAd1 Table 9: Clinical Trials with JX - 594 Table 10: Clinical Trials with GL - ONC1 Table 11: Clinical Trials
of CAVATAK (CVA21) Table 12: Clinical Trials with MV - NIS Table 13: Overview
of Oncolytic Viruses by Development Phase & Virus Family Table 14: Profile
of Approved and Marketed Oncolytic Viruses Table 15: Pivotal Study Design
of Oncolytic Viruses in Late
Stage Development Based on Previous Clinical Results Table 16: Approved Indications
of Immune Checkpoint Inhibitors Table 17: Active Clinical Studies
of Oncolytic Viruses in Combination with Immune Checkpoint Inhibitors (ICI) Table 18: Planned Clinical Studies
of Oncolytic Viruses in Combination with Immune Checkpoint Inhibitors (ICI) Table 19: Active or Planned Clinical Studies
of Oncolytic Viruses in Combination with Other Anti-Cancer Therapeutics Table 20: Pattern
of Transgenes in Oncolytic Viruses in Relation to Development Phase Tables 21a and 21b: Indications and Frquency and Way
of Administration
of Oncolytic Viruses in Active and / or Positive Completed Clinical Studies Table 22: Small and Medium Pharma & Biotech as Partner for Regional Co-Development
of Oncolytic Viruses Table 23: Immuno - Oncology Portfolio
of Major Pharma & Biotech with Interest in Oncolytic Viruses Table 24: Interests
of Major Pharma & Biotech in Oncolytic Viruses Table 25: First Generation Oncology Virus Companies and their Sources
of Technology Table 26: Second Generation Oncology Virus Companies and their Sources
of Technology Table 27: Third Generation Oncology Virus Companies and their Sources
of Technology Table 28: Fourth Generation Oncology Virus Companies and their Sources
of Technology Table 29: Grants, Credits & Donations Table 30: Financing by Venture Capital, Private Equity and Other Private Placements Table 31: Collaboration & Licensing Agreements Table 32: Companies Listed on Stock Exchange & Offerings Table 33: Mergers & Acquisitions
But there's another group
of PD symptoms, termed the «non-motor symptoms» (NMS)
of PD, that gets far less attention, even though NMS begin to manifest earlier in the
disease, are harder to treat with
current therapies, and include some
of the most crippling features
of living with the later
stages of PD.
The
current project utilized an array
of immunochemical and molecular tools to perform a characterization
of retinal pathology in the early
stages of disease progression using a well - validated mouse model
of AD (APPSWE / PS1ΔE 9).
It's life cycle involves an egg which develops into larval
stage (6 weeks feeds on rodents and birds), then nymph (8 weeks this is believed to be the cause
of Lyme
disease in people also feeds on other mammals), then adult tick (
current belief is that this is the cause
of Lyme in the dog and feeds on other mammals).
Medical experts have noted that patients in the early
stages of chronic kidney
disease are at increased risk for clinical depression according to the study in the
current issue
of the American Journal
of Kidney Diseases.