Allan Robins, Ph.D., Senior Vice President of Science and Technology, will review recent progress with the company's VC - 01 ™ product candidate for the treatment of type 1 diabetes, which entered
the clinical phase of development late last year.
Dr. Brandon will review recent progress with the company's VC - 01 ™ product candidate for the treatment of type 1 diabetes, which recently entered
the clinical phase of development.
Dr. Laikind will review recent progress with the company's VC - 01 ™ islet replacement product candidate for the treatment of type 1 diabetes, which recently entered
the clinical phase of development.
Not exact matches
Cambridge, MA — March 30, 2017 — Aura Biosciences, a biotechnology company developing a new class
of therapies to target and selectively destroy cancer cells using viral nanoparticle conjugates, announced today that it has enrolled and dosed the first patient in its
Phase 1b
clinical trial
of light - activated AU - 011, an investigational, first - in - class targeted therapy in
development for the treatment
of ocular melanoma, a rare and life - threatening disease.
This includes a stem cell research centre, a network
of drug discovery institutes and a # 20 million global
clinical development fund dedicated to supporting
Phase I and II
clinical trials; and a # 2 million collaboration between University
of Cambridge and University College London that will use donated cells from people with Alzheimer's to test potential new treatments
For example, you might make a list
of 20 or 30 companies, all with cancer drugs in
Phase II
of clinical development.
But highly trained life scientists will still be needed for such tasks as late - stage
development (ensuring smooth implementation
of final
phase (III and IV)
clinical trials) as well as compliance with regulatory demands (so - called commissioning and validation specialists), according to Croonen.
Last month, Biopure launched a revamped
clinical development program, emphasizing testing in Europe, with three
phase II
clinical trials planned for 2008 to study the impact
of its product on heart attack patients, chemotherapy patients with anemia and the terminally ill.
The documentation ranges across the whole spectrum
of drug
development: Investigators» brochures provide information on all that is currently known about the medicine and so need periodic updating; accurate and concise protocols are required to ensure that trials are performed effectively;
clinical trial reports (generally from
phase II and III studies) present the information gathered from the trials; higher level documents provide summaries
of efficacy and safety data from
clinical trial programmes; expert reports provide critical interpretation
of the results; and response documents clarify any points that are not clear to the regulatory agencies or provide additional analyses or supporting data for any items
of concern.
However, RA professionals are increasingly involved with products during the research and
development phases, in the design and monitoring
of clinical studies, marketing, advertising, and communications.
Her research at Stanford University has contributed to the
development of a small molecule peptide that is currently in
Phase IIA
clinical trials for AD.
Development of a second CETP inhibitor, dalcetrapib, was stopped when a
phase 2
clinical trial found the drug to be ineffective.
The authors believe that the incorporation
of such a blood test into routine
clinical practice could provide a prime opportunity for intervention during the pre-cancerous
phase before the
development of pancreatic malignancy.
The
phase in the
development of a new treatment where
clinical trials are conducted using many patients, to determine whether the treatment is effective
P - BCMA - 101 is Poseida's lead CAR - T therapy currently in
Phase 1
clinical development for the treatment
of multiple myeloma.
Research Interests:
Clinical pharmacology
of anticancer agents; early
phase drug
development; drug tolerability in cancer patients with HIV / AIDS; drug tolerability in cancer patients with organ dysfunction; blood - brain barrier penetration
of drugs.
She is CEO
of PsychoGenics Inc., a profitable preclinical CNS service company, CEO
of PGI Drug Discovery LLC, a company engaged in psychiatric drug discovery with three partnered
Phase II
clinical programs and Adjunct Associate Professor
of Neuroscience at Mount Sinai School
of Medicine, Dr. Leahy has more than 25 years
of experience in drug discovery,
clinical develop and business
development for pharmaceutical and biotechnology companies, including extensive knowledge
of technology assessment, licensing, mergers and acquisitions, and strategic planning.
GenIbet's core activity is the manufacture and supply
of materials for use in early stage drug
development, pre-
clinical studies and cGMP manufacturing from
Phase I to
Phase III
clinical trials.
Once this
development culminated in the product
of the successive
phases of clinical trials, for a provision
of patients.
The company's lead product is for the personalized treatment
of advanced renal cell carcinoma and is in
phase III
clinical development.
Reykjavik, ICELAND, December 17, 2004 — deCODE genetics (Nasdaq: DCGN) today announced the signing
of an agreement under which it will conduct a
Phase II information - rich
clinical trial next year
of a third - party compound as part
of a drug
development program in asthma.
We have completed the active
phase of a Phase 1 trial of a Vaxwave ® - based vaccine against cytomegalovirus (CMV) and are finalizing clinical development plans for TheraT ® in Human Papilloma Virus (HPV)- related head and neck can
phase of a
Phase 1 trial of a Vaxwave ® - based vaccine against cytomegalovirus (CMV) and are finalizing clinical development plans for TheraT ® in Human Papilloma Virus (HPV)- related head and neck can
Phase 1 trial
of a Vaxwave ® - based vaccine against cytomegalovirus (CMV) and are finalizing
clinical development plans for TheraT ® in Human Papilloma Virus (HPV)- related head and neck cancers.
Asterias has received a Strategic Partnerships Award grant from the California Institute for Regenerative Medicine, which provides $ 14.3 million
of non-dilutive funding for the
Phase 1 / 2a
clinical trial and other product
development activities for AST - OPC1.
A concentrated source
of information on cell therapies spanning the different stages
of development: including research, pre-
clinical,
clinical and marketed
phases, being pursued by both non-profit organizations (NPO) and industries.
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
Finally, the plans for the future
development of the vaccine and the next steps to
phase II
clinical trial were presented.
We believe this finding will assist us in designing the next
phase of clinical development, in which DG031 will be studied for the prevention
of heart attack.»
Texas Children's Cancer Center is a member
of the COG
Phase I Consortium, a small and select group
of institutions that administer
Phase I
clinical trials
of drugs in early
development.
The
clinical biostatistics team has strong connection with the Biometry department (Head A. Savignoni), the early
phase clinical trial and precision medicine unit where patients are treated with drugs in
development (Head C. Le Tourneau), the translational research department in particular the Circulating Tumor Biomarkers laboratory (Charlotte Proudhon), and
of course the other teams
of the U900.
The scientific goal
of the Developmental Cancer Therapeutics Program is to discover and characterize unique agents and pathways that will impact the
development of more effective cancer therapies and to translate these discoveries into
clinical applications by using proof -
of - principle, early
phase clinical and correlative science studies.
Overall, SR - Tiget represents a multi-disciplinary research environment, which provides a unique blend
of scientific expertise in the
development of innovative gene and cell therapy strategies, access to relevant preclinical models to evaluate their efficacy and safety, as well as competence in conducting early
phase clinical trials.
deCODE genetics (Nasdaq: DCGN) today announced that it has begun enrolling patients in its
Phase I
clinical development program for DG051, the company's follow - on developmental compound for the prevention
of heart attack.
Reykjavik, ICELAND, December 17, 2004 — deCODE genetics (Nasdaq: DCGN) today announced the signing
of an agreement under which it will conduct a
Phase II information - rich
clinical trial next year
of a third - party compound as part
of a drug
development program in...
Recent
clinical studies support the
development of DG041 as an effective anti-platelet that does not increase bleeding risk deCODE genetics (Nasdaq: DCGN) today announced progress in the
development of DG041, the company's
Phase II developmental compound for the...
Translational medicine is the integrated application
of innovative pharmacology tools, biomarkers,
clinical methods,
clinical technologies and study designs to improve disease understanding, confidence in human drug targets and increase confidence in drug candidates, understand the therapeutic index in humans, enhance cost - effective decision making in exploratory
development and increase
phase II success.
Essentially, Roche has committed to paying Isis $ 30 million for the
development of its Huntington's disease drugs and the first «
phase 1»
clinical trial in patients.
The positive results from the two
phase III studies
of ipilimumab were made possible in part through the evolution
of the
clinical science, which is based on new models
of academic - industry partnership to advance immunotherapy
development.
GENYO is the first national centre devoted to genomics that integrates the Public Administration, the University and the biotechnology and pharmaceutical business sector, which would allow the integration
of research in all its
phases, from the generation
of knowledge to its
development in
clinical and pharmaceutical applications, the
development of new projects and services for the prevention, diagnosis and treatment
of diseases associated to human genetic variability, such a cancer and rare diseases, diabetes, hypertension or degenerative diseases, among others.
Lilly Halts
Development of Semagacestat for Alzheimer's Disease Based on Preliminary Results
of Phase III
Clinical Trials.
That's when I started working as an Associate
Clinical Project Manager in the Late
Phase area
of Clinical Development.
Approved programs demonstrate responsibility for the quality
of candidates by ensuring that
development of candidate quality is the goal
of educator preparation in all
phases of the program — from recruitment, at admission, through the progression
of courses and
clinical experiences — and in decisions that program completers are prepared to be effective educators and are recommended for certification.
BioMS is in a
clinical development phase with a
phase - two and a couple
of phase - three
clinical trials going on, which means that there are
clinical - trial agreements, indemnification agreements, budget - amendment agreements, as well as research and
development contracts with outside agencies and those with outside consultants.
Practical knowledge
of GMP and an ability to apply sound judgment and decision - making skills (risk based and appropriate for the
phase of clinical development) in order to evaluate product release.
Worked in a
Phase I / II
clinical trials research laboratory that focuses on the
development of antigen - specific cytotoxic T - lymphocytes for adoptive cellular immune therapies in children and adults
Past successes have included
development and
clinical characterization
of biologics (anti-IL10 and 23 neutralizing antibodies -
Phase III) along with small molecule antagonists (HCV - «Boceprevir» and BACE (
Phase I - III
clinical development)-RRB-.
Summary: This project involved
development and testing thoroughly the concepts
of phase 1
of Clinical Acces...
Areas
of Clinical Interest: Women's Issues, Adolescent & Child
Development, Disordered Eating Issues, Depression, Anxiety, College Students, Creative Individuals,
Phase of Life / Adjustment Transitions, Cultural Issues.
Family Healing, coauthored with Michael Nichols, blends vignettes from Minuchin's personal history with
clinical cases to illustrate his understanding and treatment
of families throughout various
phases of family
development.