Wider Reach, Stronger Studies
Our extensive network of engaged patients assures you of access to hard-to-reach populations affected by genetic disorders. We strategically recruit the most eligible participants and increase study retention by taking biospecimen and data collection directly to the patient’s home. As a fully integrated services solution, you can expect streamlined logistics that allow you to focus on advancing the next therapy instead.
- Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC)
- Cystic Fibrosis (CF)
- Down Syndrome (Trisomy 21)
- Duchenne Muscular Dystrophy (DMD)
- Glucose-6-phosphate-dehydrogenase (G6PD)
- Hereditary Hemorrhagic Telangiectasia (HHT)
- Hunter’s Syndrome (MPS II)
- Huntington's Disease (HD)
- Myotonic Dystrophy
- Spinal Muscular Atrophy
Sanguine's Expertise in Genetic & Rare Diseases
>800
Patient Members
>25
Studies Completed
Contact us to discuss your research needs
Sanguine Services
- Single Timepoint - Huntingtons
- Ability to consent and enroll pediatric patients
- Connect with hard to reach patients / rare disease patients
- Access to patients via patient advocacy groups and non-profit organizations
- PBMC isolation
- "Treatment naive (eg: no disease-modifying therapies)"
- Identify specific mutations and genotypes
- Enzyme deficiency
- Familial history
- Whole Blood
- Serum
- Plasma
- Urine (Ex: Lupus nephritis)
- Skin Taping (ex: Atopic dermatitis)
- DNA/RNA
- PBMCs (+ Derivatives)
- Hair
- Stool
- Semen
- Nails
- Buffy Coat
- Disease Confirmation
- Covid-19 (PCR)
- Sickle Cell
- HIV/HPV/Hepatitis/Herpes Etc.
- BioMarker Quantification
- CBC, Platelett, & Diff
- CRP
- Cal-Protecin
- ANA
- Cytokine Panel
- BUN
- Urinalysis
- Thyroid Stimulating Hormone
- Lipid Panel
- LDH
- Genetic Analysis
- HLA Typing
- dsDNA
- RNA Vial Load Qaunitification
- HBV Genotyping
Growing insight into the molecular origins of genetic disorders has allowed biomedical science to stand on the cusp of many new treatments finally reaching patients in need. To augment therapeutic development, we ensure you’re working with a sufficient sample size and have a comprehensive view of people living with a genetic disorder. As a partner that is also attuned to the unique study design and privacy requirements necessitated in this field, we enable new opportunities for you to improve patients’ wellbeing faster.
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