Rare Diseases Clinical Research Consortia (RDCRC) RFA-OD-08-001 for Rare Diseases Clinical Research Network

 

ICs Areas of Research Interest and Program and Grants Management Contact Information

 

National Cancer Institute (NCI)

 

The NCI seeks clinical research teams studying rare cancers.  Examples include, but are not limited to the following rare cancers: carcinoid, primary CNS-lymphoma, sarcomas, and urinary bladder cancer.

 

NCI Program Contact:

 

Elizabeth Read-Connole, Ph.D.

NCI Representative to Office of Rare Diseases Committee
Cancer Etiology Branch,
Division of Cancer Biology
National Cancer Institute, NIH
6130 Executive Plaza North Room 5016
Bethesda, MD 20892-7398
301-496-6085 (phone)
301-496-2025 (Fax)
bconnole@mail.nih.gov

 

Grants Management Contact:

 

Ms. Angela Urdaneta

EPS/ Room 243

6120 Executive Blvd

Rockville, MD 20892-7150

301.496.9901

urdanetaa@mail.nih.gov

National Heart, Lung and Blood Institute (NHLBI)

The NHLBI is interested in rare diseases and conditions of blood, lung and heart.  Below are some examples only, other rare heart, lung, and blood diseases may also be appropriate. Examples of rare blood diseases: Acquired aplastic anemia, Antiphospholipid syndrome, Creutzfeldt-jakob disease (CJD), Cooley’s Anemia, Fanconi Anemia, Hemophagocytic lymphohistiocytosis, Hemophilia, hereditary hemorrhagic telangiectasia (HHT), heparin-induced thrombocytopenia (HIT), Lymphedema, myelodysplastic syndrome (MDS), myeloproliferative disorders (MPD), paroxysmal nocturnal hemoglobinuria (PNH), Rare Bleeding Disorders, Rare Nutritional Anemias, Rare Thrombotic Disorders, Rare Hemolytic Anemias, Sickle cell disease, Thalassemia, Thrombocytopenias of Different Etiologies, thrombotic thrombocytopenic purpura (TTP). Examples of rare lung diseases:Alpha-1-Antitrypsin deficiency (A1AT), Alveolar proteinosis, Congenital cysts and lobar emphysema, Congenital hypoventilation syndromes, Congenital Lymphangiectasia, Cystic fibrosis (CF), Idiopathic pulmonary arterial hypertension, Idiopathic pulmonary fibrosis (IPF), Lymphangioleiomyomatosis (LAM), Pediatric interstitial lung disease, Primary ciliary dyskinesia (PCD), Sarcoidosis, Surfactant protein deficiencies. Examples of rare heart diseases: Marfan Syndrome , Peripartum Cardiomyopathy , Inherited channelopathies (Long-QT Syndrome, Brugada Syndrome) , Rare Inherited Cardiomyopathies (Arrhythmogenic Right Ventricular Dysplasia) , Hereditary Hemorrhagic Telangectasia (HHT), Supravalvular Aortic Stenosis (SVAS), Klippel-Trenaunay-Weber Syndrome (KTWS).  A list of rare diseases that are relevant to the research mission of the NHLBI can be found at: http://www.nhlbi.nih.gov/funding/inits/rd_list.htm

Program Contacts:

1) For rare heart diseases:

 

Sonia I. Skarlatos, Ph.D., FAHA 
Acting Director
Division of Cardiovascular Diseases
NHLBI Gene Therapy Coordinator
National Heart, Lung and Blood Institute
Tel: 301-435-0477
Fax: 301-480-7971

Email: skarlats@nhlbi.nih.gov

2) For rare lung diseases:

Hannah H. Peavy, M.D.

Division of Lung Diseases

National Heart, Lung, and Blood Institute

6701 Rockledge Drive, Room 10160

Bethesda, MD 20892-7952

Phone: (301) 435-0222

Fax: (301) 480-3557

Email: peavyh@nhlbi.nih.gov

 

3) For rare blood diseases:

Andrei L. Kindzelski, M.D., Ph.D.

Medical Officer, Program Director

Division of Blood Diseases and Resources

National Heart, Lung, and Blood Institute

National Institutes of Health

6701 Rockledge Drive, MSC 7950

RKL II Building, Room 9170

Bethesda, MD 20892-7950

Tel 301-402-0658, FAX 301-480-1046

E-mail: kindzelskial@nhlbi.nih.gov

Grants Management Contact:

Robert Vinson, Jr.

Branch Chief, Blood Team

NHLBI, DERA, Office of Grants Management

Rockledge Centre Two, Suite 7044

6701 Rockledge Drive, MSC 7926

Bethesda, Maryland  20892-7926

Telephone:  (301) 435-0169

Facsimile:  (301) 451-5462

E-mail:   vinsonr@nhlbi.nih.gov

National Institute on Aging (NIA)

The NIA seeks to support clinical research in inherited disorders of premature or accelerated aging, including (but not limited to) Werner’s syndrome, Down’s syndrome, and Hutchinson-Guilford Progeria. 

 

Program Contact:

 

Susan G. Nayfield, M.D., M.Sc.

Chief, Geriatrics Branch

Geriatrics and Clinical Gerontology Program

National Institute on Aging

7201 Wisconsin Avenue

Gateway Building, Suite 3C-307

Bethesda, MD  20892-9205 

Phone:  (301) 496-6761

Fax:  (301) 402-1784

E-mail:  nayfiels@mail.nih.gov

 

Grants Management Contact:

 

Jeff Ball

Grants Management Specialist

Grants & Contracts Management Office

NIH, DHHS

National Institute on Aging (NIA)

E-mail: ballj@nia.nih.gov 

National Institute on Alcohol Abuse and Alcoholism (NIAAA)

The NIAAA is interested in alcohol-related rare digestive diseases including liver steatosis, hepatic fibrosis, hepatocellular carcinoma, hepatorenal syndrome, and chronic pancreatitis. Progress in early diagnosis and treatment of these diseases has been limited by a poor understanding of their pathogenesis. Further clinical studies analyzing various risk factors such as diet, patterns of drinking, viral and bacterial infection, as well as genetic and epigenetic factors, are needed to facilitate better and earlier diagnosis and management of each of these diseases.

 

Program contact:

 

Svetlana Radaeva, Ph.D.

5635 Fishers Lane, Room 2033

Bethesda, MD 20892-9304

Tel: 301-443-1189

Fax: 301-594-0673

Email: sradaeva@mail.nih.gov

 

Grants Management contact:

 

Judy S. Fox

Chief, Grants Management Branch

Chief Grants Management Officer, NIAAA

5635 Fishers Lane, Room 3023, MSC 9304

Bethesda, MD  20892-9304

FOR EXPRESS MAIL:  Rockville, MD  20852-1705

Phone:  301-443-4704

FAX:  301-443-3891

Email:  jfox@mail.nih.gov

 

National Institute of Allergy and Infectious Diseases (NIAID)

NIAID research activities on rare diseases are classified into four areas: infectious diseases, primary immunodeficiency diseases, autoimmune diseases, and allergic diseases. NIAID's section of this report highlights the Institute's rare diseases advances and activities.

·         Infectious diseases include diseases caused by bacteria, parasites, viruses, and fungi. Research on rare infectious diseases is aimed at delineating mechanisms of disease pathogenesis and developing more effective diagnostic, treatment, and prevention strategies.

·         Primary immunodeficiency diseases are hereditary disorders caused by intrinsic defects in the cells of the immune system and are characterized by unusual susceptibility to infection. NIAID research is focused on the development of technology to make gene transfer an effective and curative therapy, and on the identification of gene defects and immunologic abnormalities that lead to defective function.

·         Autoimmune diseases are diseases in which the immune system mistakenly attacks and damages the body's own cells and tissues. NIAID research is focused on the identification of mechanisms of pathogenesis and the development of new approaches to prevention and treatment.

·         Allergies are inappropriate or exaggerated reactions of the immune system to substances that cause no symptoms in the majority of people. NIAID research is focused on the development of new approaches for the diagnosis, prevention, and treatment of allergic diseases.

Program Contact:

Josiah Wedgwood MD PhD

Division of Allergy Immunology & Transplantation, NIAID

6610 Rockledge Drive

Room 3019, MSC 6601

Bethesda, MD  20892

(for Federal Express 20817)

Tel.:   301-496-7104

Fax:    301-480-1450

Email:  JWedgwood@niaid.nih.gov

Grants Management Contact:

Victoria Connors
Branch Chief, Grants Management Program, NIAID
6700B Rockledge Drive
Room 2122, MSC 7614
Bethesda, MD 20892-7614
Tel.: 301-402-5601
Fax: 301-493-0597
Email: connorsv@niaid.nih.gov

National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)

Many arthritic, rheumatic, musculoskeletal and skin diseases affecting adults and children that are of importance to NIAMS are considered rare.  NIAMS is interested in supporting research into the causes, treatment and prevention of these rare diseases.

 

Program Contact: 

 

James Witter MD, PhD

Medical Officer

National Institute of Arthritis and

Musculoskeletal and Skin Diseases (NIAMS)

National Institutes of Health

6701 Democracy Blvd.  Suite 800

Bethesda, MD 20892-4872

phone: 301-594-1963

fax: 301-480-4543

witterj@mail.nih.gov

 

Grants Management Contact:

 

Melinda Nelson

Chief Grants Management Officer

National Institute of Arthritis and

Musculoskeletal and Skin Diseases (NIAMS)

National Institutes of Health

6701 Democracy Blvd., Suite 800

Bethesda, MD 20892-4872

Phone: (301) 435-5278

E-Mail: MN@23Z@NIH.GOV

 

 

National Institute of Child Health and Human Development (NICHD)

 

The NICHD conducts and supports research on topics related to health of children, adults, families, and populations.  Many disorders that affect children and their families are rare diseases; NICHD currently supports research in a least 80 rare disorders. Many of those rare diseases have a genetic basis.  NICHD encourages applications in rare disorders, such as metabolic disorders (e.g., urea cycle disorders, amino acidurias, mitochondrial disorders, disorders of cholesterol metabolism, disorders of steroid metabolism), chromosomal syndromic disorders (e.g., Angelman, Prader Willi, Rett, Williams, Smith-Magenis, Cornelia de Lange, DiGeorge, 18q,1q.), storage diseases (e.g., lysosomal storage diseases, gangliosidoses, mucopolysaccharidoses, mucolipidoses, peroxisomal disorders, etc.), muscular dystrophies, sex chromosome disorders (Turner syndrome, Klinefelter syndrome, XXYY, XXXY, XYY), and other X-linked and autosomal disorders. 

 

Program Contact:

 

Mary Lou Oster-Granite, Ph. D.

Health Scientist Administrator

Mental Retardation and Developmental Disabilities Branch

Center for Developmental Biology and Perinatal Medicine

National Institute of Child Health and Human Development

National Institutes of Health

Room 4B05L, MSC 7510

6100 Executive Boulevard

Bethesda, MD 20892-7510

Telephone: 301-435-6866

FAX: 301-496-3791

E-mail: mo96o@nih.gov

 

Grants Management Contact:

 

Bryan S. Clark, M.B.A

Chief Grants Management Officer

Grants Management Branch, NICHD

Room 8A01, MSC 7510

6100 Executive Blvd.

Telephone: 301-435-6971

Fax: 301-402-0915

 

National Institute of Dental and Craniofacial Research (NIDCR)

 

The NIDCR is interested in rare oral and craniofacial diseases and disorders. Examples include:

I)                     Rare tumors of head and neck: oral cancer, salivary gland cancers etc.;

II)                   Diseases with associated tooth defects: Amelogenesis imperfecta variants and Dentinogenesis imperfecta variants; Diseases associated with hypodontia (Ectodermal Dysplasias);

III)                  Diseases with associated periodontitis: Hereditary gingival fibromatosis; Periodontitis associated with metabolic, structural or immune protein defects (Papillon-Lefevre syndrome, Cathepsin C mutations, Ehlers–Danlos syndrome type 4, and Ehlers–Danlos syndrome type 8); Periodontitis associated with severe congenital neutropenias; Periodontitis associated with abnormal neutrophil function

 

Program Contact:

 

Yasaman Shirazi, Ph.D.

Program Director,

Epithelial Cell Regulation and Transformation Program

Integrative Biology and Infectious Diseases Branch

National Institute of Dental and Craniofacial Research (NIDCR), NIH

6701 Democracy Boulevard, RM: 620

Bethesda, Maryland  20892-4878 (Courier, 20817)

Tel:  301-594-4812

Fax: 301-480-8319

Email: Yasaman.shirazi@nih.gov

 

Grants Management Contact:

 

Mary Daley

Chief, Grants Management Branch

National Institute of Dental and Craniofacial Research

Building 45, Room 4AN 44B

45 Center Drive

Bethesda, MD 20892-6402

Voice: (301) 594-4808

Fax: (301) 480-3562

Email: Daleym@mail.nih.gov

 

National Institute of Diabetes and Digestive and kidney Diseases (NIDDK)

 

The NIDDK supports research on rare diseases and conditions resulting in endocrine, metabolic, digestive, hematologic and kidney disorders.  Below are some examples of rare diseases that may be appropriate. Rare digestive diseases would include liver, pancreas and gastrointestinal diseases. Example of bowel diseases include Inflammatory Bowel Diseases (IBD) in children, including Crohn’s disease, with subphenotypes of small bowel only or colon only disease, ulcerative colitis, with subphenotypes of limited colitis and pan colitis, and patients with indeterminate colitis. Examples of rare metabolic diseases include aminoacidopathies, cystic fibrosis, lysosomal storage diseases, and urea cycle defects.  Examples of rare hematologic and kidney diseases include inherited and acquired systemic amyloidosis, inherited bone marrow failure syndromes (e.g. Diamond-Blackfan Anemia, Dyskeratosis Congenita, Schwachman-Diamond Syndrome, Fanconi Anemia, Amegakayocytic Thombocytopenia, and Severe Congenital Neutropenia), oxalosis, and tuberosclerosis.

Program Contact

Catherine McKeon, Ph.D.
Senior Advisor for Genetic Research
National Institute of Diabetes and Digestive and Kidney Diseases
Room 6103 Democracy 2
6707 Democracy Blvd. MSC 5460
Bethesda, MD 20892-5460 ( For FedEx 20817)
301-594-8810
301-480-3503 (FAX)

Email: cm67w@nih.gov

Grants Management Contact:

 

Mary K. Rosenberg

Section Chief, DEM Team

Grants Management Branch, NIDDK

Democracy Plaza II, Room 745

6707 Democracy Blvd. MSC 5456

Bethesda, MD 20892 (express mail zip 20817)

301-594-8891

Fax: 301-594-9523

Email: RosenbergM@extra.niddk.nih.gov

National Institute of Neurological Disorders and Stroke (NINDS)

The NINDS seeks to support clinical research on rare disorders that affect the central and peripheral nervous systems. Examples of groupings of rare neurological conditions would include lysosomal storage disorders, leukodystrophies, channelopathies, dystonia and other movement disorders, ataxias, muscular dystrophies, motor neuron disorders, mitochondrial encephalopathies, and brain malformations but interest is not limited to these conditions. A list of diseases that is relevant to the research mission of the NINDS can be found at http://www.ninds.nih.gov/disorders/disorder_index.htm.

 

 

Program Contacts:

 

1) Danilo A. Tagle, Ph.D.

National Institute of Neurological Disorders and Stroke

National Institutes of Health

6001 Executive Boulevard, Room 2114

Bethesda, Maryland 20892-9525

Telephone: (301) 496-5745

Fax: (301) 402-1501

Email: tagled@ninds.nih.gov

 

2) Randall R. Stewart, Ph.D.

Program Director for Channels, Synapses and Circuits

SBIR/STTR Program Coordinator

National Institute of Neurological Disorders and Stroke

National Institutes of Health

Neuroscience Center, Room 2135

6001 Executive Blvd.

Bethesda, MD 20892-9523

(For courier delivery:  Rockville, MD 20852)

Telephone 301-496-1917

Fax 301-402-1501

e-mail stewartr@ninds.nih.gov

 

Grants Management Contact:  

 

Tijuanna Decoster

Chief, Grants Management Branch

National Institute of Neurological Disorders and Stroke

National Institutes of Health

6001 Executive Blvd, Room 3258, MSC 9537

Bethesda, MD 20892-9537

Telephone:   (301) 496-9231

Fax: (301) 402-0219

Email:   td18k@nih.gov