№ lp_1_2_49293
File format: docx
Character count: 2349
File size: 73 KB
Note:
Year
Topic:
Neurology, Parkinson’s Disease
Document Type:
Request for Applications
Price: 8 / 10 USD
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Year:
2025
Region / City:
Singapore
Topic:
Target Validation, Drug Discovery
Document Type:
Call for Proposals
Organization:
Singapore Therapeutics Development Review (STDR)
Author:
N/A
Target Audience:
Researchers, Principal Investigators, Institutions
Period of Action:
2025
Approval Date:
N/A
Date of Last Changes:
N/A
Year:
2024
Region:
Africa
Document type:
Call for Expression of Interest (EOI)
Issuing organizations:
Africa CDC, Unitaid
Target audience:
Pharmaceutical manufacturers, CDMOs, CROs in Africa
Programmatic focus:
Maternal health, malaria, HIV, and related co-infections
Submission deadline:
August 15, 2024
Question deadline:
July 30, 2024
Issue date:
July 8, 2024
Supported interventions:
Safe Birth Africa project co-funded by European Union
Scope:
Regional manufacturing of therapeutics, diagnostics, and APIs
Product categories:
Oral solid dosage forms, sterile injectables, APIs
Year:
Not specified
Region / city:
Not specified
Theme:
Parkinson’s disease, therapeutic research
Document Type:
Pre-Clinical Proposal Template
Organization / Institution:
Michael J. Fox Foundation
Author:
Not specified
Period of validity:
Not specified
Approval Date:
Not specified
Modification Date:
Not specified
Date:
April 22nd, 2025
Region / City:
Paris, France
Subject:
Immuno-oncology, Biotechnology
Document Type:
Press Release
Organization / Institution:
Egle Therapeutics
Author:
Egle Therapeutics
Target Audience:
Medical and scientific professionals in immuno-oncology and biotechnology
Period of Activity:
2025
Date of Approval:
April 22nd, 2025
Date of Changes:
N/A
Year:
Not specified
Region / city:
Not specified
Document Type:
Request for Applications
Organization / institution:
Not specified
Author:
Not specified
Target audience:
Researchers in Parkinson’s disease therapeutics
Period of validity:
Not specified
Approval date:
Not specified
Amendment date:
Not specified
Year:
2024
Region / city:
United States
Subject:
COVID-19 therapeutics development
Document type:
Request for Proposals (RFP)
Organ / institution:
Biomedical Advanced Research and Development Authority (BARDA)
Author:
Biomedical Advanced Research and Development Authority (BARDA)
Target audience:
Product developers, biomedical organizations
Period of validity:
2024–2027
Approval date:
05 August 2024
Amendment date:
20 August 2024
Note:
Year
Subject:
Gene Transfer, Targeting, and Therapeutics
Document Type:
Request Form
Organization / Institution:
Salk Institute
Target Audience:
Researchers and Lab personnel
Context:
A form for requesting viral vectors from the Gene Transfer, Targeting, and Therapeutics Facility at the Salk Institute for scientific research purposes.
Year:
2026
Region / City:
La Jolla, CA
Topic:
Gene Transfer, Viral Vectors
Document Type:
Request Form
Organization / Institution:
Salk Institute for Biological Studies
Author:
GT3 Core Facility
Target Audience:
Researchers, Investigators
Validity Period:
N/A
Approval Date:
N/A
Modification Date:
N/A
Year:
2013
Region / city:
Gauteng Province
Theme:
Pharmaceuticals, Therapeutics, Rational Medicine Use
Document type:
Educational material
Institution:
Management Sciences for Health (MSH)
Author:
Management Sciences for Health
Target audience:
Healthcare practitioners, policy makers, and managers
Period of validity:
Indefinite
Approval date:
Not specified
Date of changes:
Not specified
Year:
2024
Region / city:
United States
Theme:
Gastrointestinal pharmacology, infectious diseases, antibiotic resistance, healthcare management
Document Type:
Review
Institution:
Hackensack Palisades Medical Center, Augusta University
Author:
Nagesh VK, Tran HHV, Elias D, Kianifar Aguilar I, Sethi T, Menon A, Mansour C, Furman F, Tsotsos K, Subar T, Auda A, Sidiqui A, Lamar J, Wadhwani N, Dey S, Lo A, Atoot A, Weissman S, Sifuentes H, Bangolo AI
Target Audience:
Healthcare professionals, researchers, medical practitioners
Period of Validity:
Ongoing studies, review is relevant until new treatments emerge
Date of Approval:
2024-07-25
Date of Changes:
2024-07-21
Facility:
Gene Transfer, Targeting and Therapeutics Facility
Institution:
Salk Institute for Biological Studies
Document Type:
Viral Vector Request Form
Subject:
Stock Reporter Viral Vectors
Submission Method:
Email to [email protected]
Required Information:
Principal Investigator, Lab Contact, Order Date, Fund Number or PO Number, Billing and Shipping Address
Aliquot Size AAV:
25 µl
Aliquot Size Lentiviral, Retroviral, Rabies:
5 µl
Vector Categories:
rAAV, Cre, DIO, FLEX, DO, Lentivirus, AAV Serotype Kits
Source References:
Addgene; Deisseroth Lab (Stanford University)
Material Transfer Requirement:
MTA required for Deisseroth Lab vectors
Titer Information:
Representative lot titers provided; actual titers may vary
Year:
2015
Region / City:
Southeastern/Southwest United States
Field:
Medicine, Oncology
Document Type:
Abstract
Organization:
Texas Tech University Health Sciences Center, University of Pennsylvania
Author:
Paul Trippier, Kshitij Verma, Tianzhu Zang, Trevor M. Penning
Target Audience:
Researchers, Medical Professionals
Effective Period:
Not specified
Approval Date:
Not specified
Date of Last Update:
Not specified
TRABECTEDIN, Powder for I.V. infusion 0.25mg, 1mg Yondelis®, Specialised Therapeutics Pharma Pty Ltd
Year:
2021
Region / City:
Australia
Topic:
Medical treatment, Oncology
Document type:
Submission
Organization / Institution:
Specialised Therapeutics Pharma Pty Ltd
Author:
Specialised Therapeutics Pharma Pty Ltd
Target audience:
Healthcare professionals, medical practitioners
Period of validity:
2021–present
Approval date:
21 April 2021
Modification date:
None
Registration status:
TGA approved
Condition:
Leiomyosarcoma (LMS)
Indication:
Advanced (unresectable and/or metastatic) leiomyosarcoma
Treatment phase:
Initial treatment, continuing treatment, and grandfather treatment
Price:
Public hospital: $8,962.05; Private hospital: $9,126.95
Prescriber type:
Medical practitioners, nurse practitioners
Restriction type:
Authority Required – Streamlined
Special pricing arrangements:
Yes
Administrative advice:
Not PBS-subsidised for inpatient use in public hospitals
Clinical criteria:
Must have received prior chemotherapy treatment including anthracycline
Population criteria:
Patients aged 18 years or older
Epidemiology:
Advanced soft tissue sarcoma
Methodology:
Cost-minimisation analysis compared to pazopanib
HRQoL:
Health-related quality of life assessed via MD Anderson Symptom Index
Outcome measures:
Progression-free survival, overall response rate, overall survival, time to progression
Comparator:
Pazopanib
Clinical claim:
Trabectedin is non-inferior in terms of safety compared to pazopanib for LMS treatment
Year:
2026
Region / city:
Switzerland
Theme:
Energy, Economy, Society
Document type:
Pre-proposal
Institution:
Swiss Federal Office of Energy (SFOE)
Author:
Unknown
Target audience:
Researchers, project coordinators, and funding institutions
Period of validity:
2025-2026
Approval date:
Not specified
Date of changes:
Not specified
Year:
2026
Region / city:
European Union
Topic:
Personalized Medicine for Cardiovascular, Metabolic, and Kidney Diseases
Document type:
Pre-proposal application form
Organization / Institution:
European Union Funding Agencies
Author:
Not specified
Target audience:
Research institutions, academic institutions, and industry partners
Duration:
Not specified
Approval date:
Not specified
Modification date:
Not specified
Contextual description:
A pre-proposal application form for the CARMEN2026 joint transnational call for proposals aimed at personalized medicine for cardiovascular, metabolic, and kidney diseases.
FREEZING OF GAIT (FOG) IN PARKINSON’S DISEASE RESEARCH PROGRAM Request for Applications Pre-Proposal
Note:
Year
Document type:
Research Program Request for Applications
Organization / institution:
MJFF
Target audience:
Researchers, clinicians, industry partners
Year:
2026
Region / City:
Springdale, AR
Topic:
Research proposal, confidentiality agreement
Document Type:
Pre-proposal application, confidentiality agreement
Organization / Institution:
Cobb-Vantress, LLC
Author:
Not specified
Target Audience:
Researchers, institutions involved in scientific research
Period of validity:
Not specified
Approval Date:
Not specified
Modification Date:
Not specified
Contextual description:
This document outlines the application process and confidentiality agreement for a research proposal under the Cobb Research Initiative, including specific instructions for submitting pre-proposals.
Year:
2026
Programme:
EUP OHAMR Joint Transnational Call
Document type:
Pre-proposal application form and guidelines
Thematic focus:
Antimicrobial resistance, treatments, adherence to treatment protocols
One-Health scope:
Human Health, Animal Health, Plant Health, Environment
Call topics:
Combination antimicrobial treatments; adherence to treatment protocols; impact of veterinary and agricultural antimicrobials on AMR transmission
Targeted pathogens:
Bacteria; Fungi; Bacteria and Fungi
Eligible applicants:
Transnational research consortia
Consortium requirements:
3–6 project partners from participating countries (up to 7 under specified conditions)
Maximum project duration:
36 months
Funding framework:
National and regional funding organisations participating in the Call
Submission deadline:
2 February 2026, 13:00 CET
Submission format:
Single PDF via electronic submission tool (PT-Outline)
Issuing body:
Joint Call Secretariat and participating funding organisations
Source type:
Official call documentation defining eligibility, structure, and content of research pre-proposals within a European transnational funding programme