WebTidewater Physicians Multispecialty Group includes over 200 family medicine and specialty physicians, including advanced practice providers. Olympus Medical Research, Dynamed Clinical Research, LP d/b/a DM Clinical Research, The Woodlands, Texas, United States, 77382, J. Lewis Research Inc. / Foothill Family Clinic Draper, J. Lewis Research, Inc. / Jordan River Family Medicine, Velocity Clinical Research, Salt Lake City, Virginia Gastroenterology Clinical Research, Bellevue, Washington, United States, 98007, Port Orchard, Washington, United States, 98366, MultiCare Institute for Research & Innovation, Wenatchee, Washington, United States, 98801, Wauwatosa, Wisconsin, United States, 53226, Hospital Militar Central Cirujano Mayor Dr. Cosme Argerich. This is a Phase 3, randomized, observer-blinded study to evaluate the efficacy, safety, tolerability, and immunogenicity of a quadrivalent influenza modRNA vaccine (qIRV) encoding HA of 4 seasonally recommended strains (2 A strains and 2 B strains) compared to licensed quadrivalent influenza vaccine (QIV) in healthy adults 18 years of Redness and swelling were measured and recorded in measuring device units. For general information, Learn About Clinical Studies. 21st Century Oncology - Florida / Candel Therapeutics, Inc. A1 Clinical Network Spring, TX (Advarra), AB Clinical Trials Las Vegas, NV (Advarra), Accel Research Sites Birmingham, AL (Advarra), Accel Research Sites Decatur, GA (Advarra), Accel Research Sites DeLand, FL (Advarra), Accel Research Sites Lake Oconee, GA (Advarra), Accel Research Sites Lakeland, FL (Advarra), Accel Research Sites Maitland, FL (Advarra), Accel Research Sites Nona Pediatric Center Orlando, FL (Advarra), Accel Research Sites St. Petersburg, FL (Advarra), Accel Research Sites Tampa, FL (Advarra), Accel Research Sites Network - Neurostudies (WIRB), Accel Research Sites-Angel Kids Pediatrics Jacksonville, FL (Advarra), Accel Research Sites-Birmingham CRU (WIRB), Accel Research Sites-OMNI Healthcare Melbourne, FL (Advarra), Accellacare Winston-Salem, NC (Advarra), Accellacare of Charleston Mt. Winchester, VA (Advarra), Amici Clinical Research Hoboken, NJ (Advarra), Amici Clinical Research Raritan, NJ (Advarra, Angeles Clinic and Research Institute (WIRB), Ann & Robert H. Lurie Children's Hospital of Chicago, Ann & Robert H. Lurie Childrens Hospital of Chicago Chicago, IL (Advarra), Applied Genetic Technologies Corp. (AGTC), Applied Genetic Technologies Corp. (AGTC), Cambridge, Applied Research Center of Arkansas (WIRB), ARC Clinical Research at Kelly Lane - Pflugerville, TX (Advarra), ARC Clinical Research at Wilson Parke Austin, TX (Advarra), Arizona Arthritis and Rheumatology Research, Inc. (Advarra), Arizona Oncology Associates, PC HGT (CBS), Arizona Retina and Vitreous Consultants (Advarra), Ark Clinical Research - Tustin, CA (Advarra), Ark Clinical Research Long Beach, CA (Advarra), Arkansas Childrens (Health System)/ Arkansas Children's Research Institute, Arkansas State University at Jonesboro, (ASU, Jonesboro), Arlington Dermatology Rolling Meadows, IL (Advarra), ARR Clinical Research at William Cannon Austin, TX (Advarra), Artemis Institute for Clinical Research (Advarra), Artemis Institute for Clinical Research (CBS), Artemis Institute for Clinical Research - Riverside (WIRB), Artemis Institute for Clinical Research - San Diego (WIRB), Artemis Institute for Clinical Research Riverside (CBS), Artemis Institute for Clinical Research San Diego, CA (Advarra), Arthritis & Osteoporosis Center, P.C. Except Bilirubin, other stable Grade1 abnormalities may be considered eligible by Investigator. Pain at injection site was graded as mild: Known uncontrolled coagulation disorder. As a physician-owned medical group, we place a large emphasis on selecting the most qualified and dedicated individuals interested in a medical career to help expand our team. Receipt of blood/plasma products, immunoglobulin, or monoclonal antibodies, from 60 days before study intervention administration, or planned receipt throughout the study. Any participant who has a SARS-CoV-2 RT-PCR or antigen test in the past 10 days prior to Visit 201 that has not been confirmed as negative. Healthy participants who are determined by medical history, physical examination (if required), and clinical judgment of the investigator to be eligible for inclusion in the study. This was a promotional video for the hospital. Planned chronic, systemic administration (defined as more than 14 days) of >10 mg prednisone (or equivalent)/day or any other systemic use of immunemodifying drugs during a period starting from 3 months prior to first administration of the trial vaccine and ending at the End of Study Visit (EOS). You have reached the maximum number of saved studies (100). With five award categories, the program recognizes our physicians who truly live and breathe our values.Physicians and team members joined our virtual celebration to recognize the 2021 winners of The Truly We provide the excellent care of the Mount Sinai Health System right in your Suffolk County community. WebFor your convenience, our Greenlawn location offers extended hours, easy scheduling, ample parking, greeters, and welcoming waiting areas. For general information, Learn About Clinical Studies. (Clinical Trial), Triple (Participant, Care Provider, Investigator). Innovative Research Of West Florida, Inc. Clearwater, Florida, United States, 33756, Miami Lakes, Florida, United States, 33016, Pembroke Pines, Florida, United States, 33024, Pembroke Pines, Florida, United States, 33026, Centricity Research Columbus Multispecialty, Principal Investigator: Joseph Surber, DO, Principal Investigator: Marshall L Nash, MD, Principal Investigator: Heather D Pugmire, MD, Principal Investigator: Jeffrey B Baker, MD, Principal Investigator: Nathan Richard, DO, Great Lakes Clinical Trials at Ravenswood Rheumatology, Evansville, Indiana, United States, 47714, Principal Investigator: Mohammed A Allaw, MD, Principal Investigator: Jennifer A Killion, MD, Metairie, Louisiana, United States, 70006, Principal Investigator: Robert J Jeanfreau, MD, Principal Investigator: Steven Geller, MD, Rockville, Maryland, United States, 20854, Principal Investigator: Alan R Pollack, MD, Methuen, Massachusetts, United States, 01844, Principal Investigator: Michael McCartney, MD, Principal Investigator: Mayur S Ramesh, MD, Edward A. Doisy Research Center-Saint Louis University Center for Vaccine Development, Saint Louis, Missouri, United States, 63104, Principal Investigator: Getahun Abate, MD, Saint Louis, Missouri, United States, 63141, Principal Investigator: Jeffrey P Tillinghast, MD, CPI, Grand Island, Nebraska, United States, 68803, Principal Investigator: Charles H. Harper, MD, Principal Investigator: Diana Florescu, MD, Meridian Clinical Research Associates, LLC, Principal Investigator: Brandon J Essink, MD, CPI, Midwest Regional Health Services, LLC/CCT Research, Principal Investigator: Tamara A Doehner, MD, Principal Investigator: Cornell Calinescu, MD/FAAFP/BCEM, Principal Investigator: Duane C Anderson, MD, Santa Rosa Medical Centers of Nevada/ CCT Research, Principal Investigator: Syed I Pervaiz, MD, Raritan, New Jersey, United States, 08869, Principal Investigator: Robert S Falcone, MD, Albuquerque, New Mexico, United States, 87102, Principal Investigator: Sara Friedman, MD, Principal Investigator: Christopher A Smith, MD, Principal Investigator: Suchet R Patel, MD, Principal Investigator: David Bernard, MD, Rochester, New York, United States, 14609, Principal Investigator: Matthew G Davis, MD, Cary, North Carolina, United States, 27518, Principal Investigator: Sylvia Piqueras Shoffner, MD, Charlotte, North Carolina, United States, 28209, Principal Investigator: George L Raad, MD, Greensboro, North Carolina, United States, 27408, Principal Investigator: Alexander V. Murray, MD, Raleigh, North Carolina, United States, 27609, Rocky Mount, North Carolina, United States, 27804, Principal Investigator: David Browder, MD, Statesville, North Carolina, United States, 28625, Principal Investigator: Joseph E Moran, MD, Wilmington, North Carolina, United States, 28401, Principal Investigator: Kevin D Cannon, MD, Winston-Salem, North Carolina, United States, 27103, Principal Investigator: Robert D Rosen, MD, Principal Investigator: Antoinette A Pragalos, MD, Principal Investigator: Richard B Powell, MD, Oklahoma City, Oklahoma, United States, 73111, Principal Investigator: Charles W Lunn, MD, BS, Oklahoma City, Oklahoma, United States, 73112, Principal Investigator: Carl P Griffin, MD, CPI, Principal Investigator: Robert Lockwood, MD, Camp Hill, Pennsylvania, United States, 17011, Principal Investigator: Nadar M Venkatesh, DO, Philadelphia, Pennsylvania, United States, 19107, East Greenwich, Rhode Island, United States, 02818, Principal Investigator: David L Fried, MD, Anderson, South Carolina, United States, 29621, Principal Investigator: Bradley Swenson, MD, Principal Investigator: Charles A Thompson, MD, Little River, South Carolina, United States, 29566, Principal Investigator: Tom A Christensen, MD, Knoxville, Tennessee, United States, 37938, Principal Investigator: Rickey D Manning, MD, Principal Investigator: Paul K Pickrell, MD, Principal Investigator: Irfan Muhammad, MD, Principal Investigator: Jeffrey Adelglass, MD, FACS, Principal Investigator: Mark D Carlson, MD, Principal Investigator: Harish P Thakkar, MD, Principal Investigator: Earl F Martin, MD, Principal Investigator: Marc O Anderson, MD, South Ogden Family Medicine/ CCT Research, Principal Investigator: John M Hemmersmeier, MD, Velocity Clinical Research, Salt Lake City, Principal Investigator: Barbara E Rizzardi, MD, Clinical Alliance for Research and Education Infectious Disease, Annandale, Virginia, United States, 22003-7347, Principal Investigator: Donald M Poretz, MD, Portsmouth, Virginia, United States, 23703, Principal Investigator: Banu P Myneni, DO, Principal Investigator: David S Ramstad, MD, Port Orchard, Washington, United States, 98366, Principal Investigator: Brad R Frandsen, MD, MultiCare Health System-DMOB (Deaconess Medical Office Building), Spokane, Washington, United States, 99204, Principal Investigator: Jonathan Staben, MD, Principal Investigator: Isabelle Schenkenberger, MD, Principal Investigator: Hermann Braun, MD, Principal Investigator: Frank Kaessner, MD, Principal Investigator: Andrea Guenzel, MD, IKF Institut fuer klinische Forschung Frankfurt, Principal Investigator: Marc O Kornmann, MD, Principal Investigator: Tabea Podszus, MD, Principal Investigator: Annemarie Kyhn, MD, Siteworks Zentrum fr Klinische Studien Heidelberg, Principal Investigator: Juergen R Fischer, MD, Dermatologische Gemeinschaftspraxis Dres. Fundacao de Apoio Ao Ensino, Pesquisa E Assistencia Do HCFMRPUSP - FAEPA (WIRB), Fundacao de Medicina Tropical Dr. Heitor Vieira Dourado (FMT-HVD) (WIRB), Fundacio Hospital Universitari Vall d'Hebron - Institut de Recerca (WIRB), Fundacion de Investigacion de Diego (WIRB), Future Health Research Clinic Miami, FL (Advarra), Futuro Clinical Trials, LLC McAllen, TX (Advarra), Gabrail Cancer Center Research Institute HGT (Advarra), Galenus Group Inc. Lehigh Acres, FL (Advarra), Galenus Group Inc. Manati, PR (Advarra), Gateway Clinical Trials, LLC OFallon, IL (Advarra), Geisinger Commonwealth School of Medicine, Genesis Clinical Research Tampa, FL (Advarra), GenHarp Clinical Solutions Chicago, IL (Advarra), Georgetown Lombardi Comprehensive Cancer Center HGT (CBS), Georgetown University Medical Center (GUMC), Georgia Clinical Research, LLC Lawrenceville, GA (Advarra), Global Health Research Center, Inc. (CBS), Global Health Research Center, Inc. Miami Lakes, FL (Advarra), Global Health Research Center, Inc.-Tampa, Great Lakes Clinical Trials - Gurnee (CBS), Great Lakes Clinical Trials Ravenswood Chicago. For general information, Learn About Clinical Studies. Want to step up your game this fall when it comes to cooking a healthy and flavorful soup? Choosing to participate in a study is an important personal decision. Advanced Vision Research Institute (CBS), F & T Medical Research, Inc. _Miami, FL (Advarra), Family Medical Clinic El Monte, CA(Advarra), Family Medicine Specialists - Wauconda, IL (Advarra), Family Practice Specialists / Synexus Clinical Research US, Inc. HGT (CBS), Feinstein Institute for Medical Research (Clinical), Feinstein Institute for Medical Research (Pre-Clinical), Fiel Family and Sports Medicine/CCT Tempe, AZ (Advarra), Fiel Family and Sports Medicine/CCT Research (CBS), Finger Lakes Clinical Research Rochester, NY (Advarra), Fleming Island Center for Clinical Research (CBS), Fleming Island Center for Clinical Research Fleming Island, FL (Advarra), Florida Cancer Specialists West Palm Beach HGT (CBS), Florida Cancer Specialists and Research Institute (WIRB), Florida Cancer Specialists, Sarasota Downtown (CBS). Tulsa, OK (Advarra), Vitalink Research Anderson, SC (Advarra), VitaLink Research Columbia, SC (Advarra), VitaLink Research Greenville, SC (Advarra), Vitalink Research Spartanburg, SC (Advarra), Vitreoretina Associates, PLC dba Retina Associates of Michigan (CBS), VitreoRetinal Associates, P.A. Medical City Dallas (WIRB), Texas Oncology, P.A. Family medicine is a branch of primary care that acts in a generalist function to provide personal, front-line medical care to patients. We can help you find a doctor. Clinica Privada Instituto Medico Platense S.A. La Plata, Buenos Aires, Argentina, B1900AVG, Instituto De Investigaciones Clnicas Mar Del Plata, Mar del Plata, Buenos Aires, Argentina, B7600FZO, Clinica Mayo de Urgencias Medicas Cruz Blanca S.R.L, San Miguel de Tucuman, Tucuman, Argentina, 4000, Hospital de Clinicas Presidente Nicolas Avellaneda, IMAC - Instituto Medico de Alta Complejidad, LMC Clinical Research Inc. (Clinical Pharmacology Unit), Dr. Anil K. Gupta Medicine Professional Corporation, Clinique de Mdecine Urbaine du Quartier Latin, St-Charles-Borromee, Quebec, Canada, J6E 2B4, Medical Corporation Heishinkai OPHAC Hospital, Medical Corp. Seikoukai New Medical Research System Clinic, Franciscus Gasthuis & Vlietland, location Gasthuis, Bloemfontein, FREE State, South Africa, 9301, Welkom Clinical Trial Centre (MERC WELKOM), Kempton Park, Gauteng, South Africa, 1619, Newtown Clinical Research Centre (PTY) LTD, Synexus SA- Watermeyer Clinical Research Center, Wits Vaccines & Infectious Diseases Analytics, Middelburg, Mpumalanga, South Africa, 1055, Synexus - Helderberg Clinical Research Centre - Somerset West, Cape Town, Western CAPE, South Africa, 7130, Cape Town, Western CAPE, South Africa, 7500, Somerset West, Western CAPE, South Africa, 7129. RSV A and RSV B neutralizing titers (NT), expressed as Geometric Mean Titers (GMTs), and geometric mean fold rise (GMFR). San Antonio, TX (Advarra), Urology Specialists-Carolinas Huntersville, NC (Advarra), US Food and Drug Administration, (FDA) NCTR, US Food and Drug Administration, (FDA) White Oak, USDA ARS Crop Improvement and Protection Research, USDA ARS Urbana, IL/University of Illinois at Urbana, Champaign, (UIUC), USDA Cropping Systems Research Laboratory, USDA National Veterinary Services Laboratories/Center for Veterinary Biologics, USDA, Agricultural Research Service, Forage-Animal Production Research Unit/University of Kentucky, USDA, Agricultural Research Service, Lincoln/UNL, USDA, Agricultural Research Service, Mid South Area Southern Regional Research Center, USDA, Agricultural Research Service, Pacific West Area, Western Regional Research Center, USDA, Agricultural Research Service/Kansas State University, USDA, ARS, Daniel K. Inouye Pacfic Basin Agricultural Research Center, USDA, National Center for Agricultural Utilization Research (NCAUR), USDA, Research, Education and Economics Agricultural Research Service, Beltsville, USDA, U.S. Horticultural Research Laboratory, USDA-Agricultural Research Service, Coastal Plains Soil, Water and Plant Research Center, USDA-Agricultural Research Service, San Joaquin Valley Agricultural Sciences Center, USDA-Agricultural Research Service, U.S. Listing a study does not mean it has been evaluated by the U.S. Federal Government. AstraZeneca (Previously known as MedImmune, LLC), CCP - Kids Way Hermitage, PA (Advarra), Coastal Carolina Research Center (dba Lowcountry Orthopaedics & Sports Medicine) (Advarra), Department of Veterans Affairs Medical Center, White River Junction/Dartmouth College, Department of Veterans Affairs W.S. Studies a U.S. FDA-regulated Drug Product: Studies a U.S. FDA-regulated Device Product: 1 of 4 dose levels of mIRV (either A or B Strain). Pain at the injection site, redness, and swelling, as self-reported in electronic diaries. It proposes an evidence based strategy to address the social determinants of health, the conditions in which people are born, grow, live, work Dr./McKinney, TX (Advarra), CardioVoyage 101 US Hwy. Reverse Transcriptase-Polymerase Chain Reaction (RT-PCR)-confirmed RSV A and/or RSV B- associated acute respiratory illness (ARI) is assessed. The middle 57% of Nephrology Nurse Practitioners makes between $105,404 and $166,413, with the top 86% making $290,466. Noise-induced hearing loss can have a serious impact on the way we live, which is why its important to wear hearing protection when you can. Talk with your doctor and family members or friends about deciding to join a study. You have reached the maximum number of saved studies (100). Choosing to participate in a study is an important personal decision. Family medicine is a branch of primary care that acts in a generalist function to provide personal, front-line medical care to patients. You have reached the maximum number of saved studies (100). What do you do if you miss an appointment, cancel or need to reschedule an appointment at a TPMG office? WebEarn your nursing degree in as little as 36 months, by enrolling in our Bachelor of Science in Nursing (BSN) program. We strive to make your visit as smooth as possible. Najit Technologies, Inc./ Oregon Health & Science University (OHSU). Fever, fatigue, headache, chills, vomiting, diarrhea, new or worsened muscle pain, and new or worsened joint pain, as self reported in electronic diaries. SAE was an AE resulting in any of the following outcomes or deemed significant for any other reason: death; initial or prolonged inpatient hospitalization; life-threatening experience (immediate risk of dying); persistent or significant disability/incapacity; congenital anomaly. Further details on Pfizer's data sharing criteria and process for requesting access can be found at: https://www.pfizer.com/science/clinical_trials/trial_data_and_results/data_requests. This is a Phase 3, multicenter, randomized, double-blinded, placebo-controlled study to assess the safety, immunogenicity, and efficacy of RSVpreF or placebo (1:1 randomization) in adults. Individual Participant Data (IPD) Sharing Statement: Pfizer will provide access to individual de-identified participant data and related study documents (e.g. For general information, Learn About Clinical Studies. A licensed quadrivalent influenza vaccine (QIV). Note: Healthy participants with preexisting stable disease, defined as disease not requiring significant change in therapy or hospitalization for worsening disease during the 6 weeks before enrollment, can be included. read Boston Childrens Hospital deleted a video telling parents their children may know theyre trans from the womb. A dose of qIRV encoding 2 A strains and 2 B strains at dose level 3. View this study on Beta.ClinicalTrials.gov. Inhaled/nebulized, intra-articular, intrabursal, or topical (skin or eyes) corticosteroids are permitted. This was a promotional video for the hospital. Subjects may have one or more chronic medical conditions e.g., mild to moderate underlying illnesses such as chronic cardiac diseases and chronic lung disease (asthma and chronic obstructive pulmonary disease [COPD]), congestive This was a promotional video for the hospital. Study record managers: refer to the Data Element Definitions if submitting registration or results information. Any participant who has received or plans to receive a modRNA-platform SARS-CoV-2 vaccine within 60 days of Visit 1. Quadrivalent influenza modRNA vaccine (single dose), participants 18 through 64 years of age, Quadrivalent influenza modRNA vaccine (single dose), Licensed quadrivalent influenza vaccine (single dose), participants 18 through 64 years of age, Licensed quadrivalent influenza vaccine (single dose), Quadrivalent influenza modRNA vaccine (single dose), participants 65 years of age, Licensed quadrivalent influenza vaccine (single dose), participants 65 years of age, Pain at the injection site, redness, and swelling, Fever, fatigue, headache, chills, vomiting, diarrhea, new or worsened muscle pain, and new or worsened joint pain, As elicited by investigational site staff, Biological: Quadrivalent influenza modRNA vaccine, Biological: Quadrivalent influenza vaccine. Talk with your doctor and family members or friends about deciding to join a study. Reverse Transcriptase-Polymerase Chain Reaction (RT-PCR)-confirmed RSV A and/or RSV B- associated acute respiratory illness (ARI) is assessed. Screening 12-lead ECG that, as judged by the investigator, is consistent with probable or possible myocarditis or pericarditis, or demonstrates clinically relevant abnormalities that may affect participant safety or interpretation of study results. Individuals who receive treatment with radiotherapy or immunosuppressive therapy, including cytotoxic agents or systemic corticosteroids, eg, for cancer or an autoimmune disease, or planned receipt throughout the study. Administration or planned administration of immunoglobulins and/or any blood products during a period starting from 3 months prior to first administration of the trial vaccine and during the trial. View details Medical Director of Oncology - Greenville, SC. Other medical or psychiatric condition including recent (within the past year) or active suicidal ideation/behavior or laboratory abnormality that may increase the risk of study participation or, in the investigator's judgment, make the participant inappropriate for the study. Back Suffolk & East End (43) New Jersey (2) Westchester (4) We also have multispecialty ambulatory care locations and doctors offices in many other neighborhoods. Are you experiencing pain in your heels, especially in the morning or after increased physical activity? We provide the excellent care of the Mount Sinai Health System right in your Suffolk County community. 1 dose of licensed QIV (as a control group). https://www.pfizer.com/science/clinical_trials/trial_data_and_results/data_requests. *Please select location from the dropdown, Northwell team members search and apply here. Reverse Transcriptase-Polymerase Chain Reaction (RT-PCR)-confirmed RSV A and/or RSV B- associated acute respiratory illness (ARI) is assessed. Pain at injection site was graded as mild: Redness and swelling were measured and recorded in measuring device units. Externships, Fellowships and Nurse Residency Programs, Perioperative Pre-Surgical, OR, PACU, Endoscopy. Are you looking for a healthier diet to kickstart the new year? Individuals who receive treatment with radiotherapy or immunosuppressive therapy, including cytotoxic agents or systemic corticosteroids (if systemic corticosteroids are administered for 14 days at a dose of 20 mg/day of prednisone or equivalent), eg, for cancer or an autoimmune disease, or planned receipt throughout the study. Participation in other studies involving administration of a study intervention within 28 days prior to, and/or during, participation in this study. Florida Eye Associates (CBS) 502 E New Haven Ave. Florida Eye Associates Melbourne, FL (Advarra), Florida Hospital Cancer Institute HGT (CBS), Florida International Research Center (WIRB), Florida Orthopaedic Associates Orange City, FL (Advarra), Florida Research Associates, LLC/Florida Orthopedic Associates Deland, FL, Florida Retina Institute Jacksonville, FL(Advarra), Florida Urology Partners Tampa, FL (Advarra), Floridian Clinical Research Hialeah, FL (Advarra), Floridian Clinical Research Miami Lakes, FL (Advarra), Floridian Research Institute, LLC. protocol, Statistical Analysis Plan (SAP), Clinical Study Report (CSR)) upon request from qualified researchers, and subject to certain criteria, conditions, and exceptions. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. Immunocompromised individuals with known or suspected immunodeficiency, as determined by history and/or laboratory/physical examination. We are here for you and your family. Occurrence of solicited systemic adverse events (body temperature, headache, fatigue, myalgia, nausea, chills) within 8 days after vaccination. Department of Veterans Affairs Jesse Brown VA Medical Center, Department of Veterans Affairs McGuire Veterans Administration Medical Center Richmond (VAMC), Department of Veterans Affairs Medical Center White River Junction / Dartmouth College-CGT, Department of Veterans Affairs Medical Center, Lexington KY, Department of Veterans Affairs Medical Center, Northport, Department of Veterans Affairs Medical Center, Ralph H. Johnson Department of Veterans Affairs Medical Center, Department of Veterans Affairs Medical Center, Salisbury/ Wake Forest University, Department of Veterans Affairs Medical Research Foundation/VA San Diego Healthcare System (VASDHS), Department of Veterans Affairs Michael E. DeBakey Department of Veteran Affairs Medical/ Baylor College of Medicine, Department of Veterans Affairs Nebraska-Western Iowa Health Care System, Department of Veterans Affairs New York Harbor Veteran Administration Medical Center, Department of Veterans Affairs Palo Alto Veterans Institute for Research / Stanford University, Department of Veterans Affairs Providence Healthcare System/Brown University, Department of Veterans Affairs Richard L. Roudebush Veterans Affairs/Indiana-Purdue University Indianapolis, Department of Veterans Affairs San Diego Healthcare System, Department of Veterans Affairs San Francisco Department of Veterans Affairs Medical Center, Department of Veterans Affairs South Georgia Veterans Health System/North Florida, Department of Veterans Affairs Southeast Louisiana Veterans Health Care System, Department of Veterans Affairs Southern Arizona Veterans Administration Health Care System (SAVAHCS), Department of Veterans Affairs St. Louis Healthcare System/Washington University in St. Louis, Department of Veterans Affairs Tennessee Valley Healthcare System, Department of Veterans Affairs VA St. Louis Health Care System, Department of Veterans Affairs, Administration Medical Center, Durham, NC, Department of Veterans Affairs, Central Arkansas Healthcare System, Department of Veterans Affairs, Cincinnati, Department of Veterans Affairs, Eastern Colorado Health Care System, Department of Veterans Affairs, Edith Nourse Rogers Memorial Veterans Hospital, Department of Veterans Affairs, Edward Hines Jr. Hospital, Department of Veterans Affairs, Greater Los Angeles Health Care System, Department of Veterans Affairs, Greater Los Angeles Health Care System/Greater Los Angeles Veterans Research and Education Foundation (GLAVREF), Department of Veterans Affairs, James H. Quillen VA Medical Center, Department of Veterans Affairs, James J. Peters VA Medical Center, Department of Veterans Affairs, Jerry L. Pettis Memorial Veterans Hospital, Department of Veterans Affairs, Miami VA Healthcare System, Department of Veterans Affairs, North Texas Health Care System, Department of Veterans Affairs, Palo Alto Health Care System/Stanford University, Department of Veterans Affairs, Pittsburgh Healthcare System, Department of Veterans Affairs, Sioux Falls VA Health Care System and the University of South Dakota, Department of Veterans Affairs;Boise VA Medical Center /Puget Sound Health Care Systems, DermResearch, Inc. Austin, TX (Advarra), Desert Clinical Research, LLC/CCT Research (CBS), Diablo Clinical Research, Inc. Walnut Creek, CA (Advarra), Diagnostics Research Group San Antonio, TX (Advarra), Diex Recherche Joliette, Inc. Saint-Charles-Borrome, QC (Advarra), Diex Recherche Quebec, Inc. Quebec City, QC (Advarra), Diex Recherche Sherbrooke, Inc. Sherbrooke, QC (Advarra), Diex Recherche Victoriaville, Inc. Victoriaville, QC (Advarra) Institution Type: Research, Dignity Health d.b.a. Participants who are willing and able to comply with all scheduled visits, treatment plan, laboratory tests, lifestyle considerations, and other study procedures. History of severe adverse reaction associated with any vaccine and/or severe allergic reaction (eg, anaphylaxis) to any component of the study intervention(s). A licensed live or vector-based vaccine within 30 days prior to or after trial vaccine administration. We strive to make your visit as smooth as possible. Healthy participants who are determined by medical history, physical examination (if required), and clinical judgment of the investigator to be eligible for inclusion in the study. WebWe would like to show you a description here but the site wont allow us. For other billing questions, please check our Billing Inquiries Page or contact the TPMG Central Billing Office at (757) 232-8777 or (877) 271-3810 for further assistance. The use of topical, inhaled, ophthalmic and nasal glucocorticoids is permitted. Ctr. It proposes an evidence based strategy to address the social determinants of health, the conditions in which people are born, grow, live, work Quist, Principal Investigator: Thomas Schaum, MD, Siteworks Prufzentrum Rendsburg - HNO Research GmbH, Principal Investigator: Henning Candler, MD, Principal Investigator: Charlotte von Engelhardt, MD, Intermed GmbH, Institut fuer medizinische Forschung und Arzneimittelsicherheit, Principal Investigator: Volker von Behren, MD. Any participant who has received or plans to receive a modRNA-platform SARS CoV-2 vaccine within 14 days before or after study vaccination at Visit 1. WebThis period also allows the student to be part of a research project and take on leadership roles. Testing methods and laboratory result interpretation techniques are also studied extensively. Communicate with your TPMG provider, receive test results and request in-person and telemedicine appointments through our Patient Portal. U.S. Department of Health and Human Services. (WIRB), Southwest Retina Research Center Durango, CO (Advarra), Southwest Retina Research Center, LLC (CBS), Southwestern Oklahoma State University, (SOSU), Spartanburg Medical Research Spartanburg, SC (Advarra), Spaulding Clinical Research, LLC (ADVARRA), Spaulding Rehabilitation Hospital / Mass General Brigham, Specialty Eye Institute Jackson, MI (Advarra), Spectrum Medical, Inc. Danville, VA (Advarra), Spokane Eye Clinical Research Spokane, WA (Advarra), Spokane Joint Replacement Center Spokane, WA (Advarra), Spokane Urology, P.S. With five award categories, the program recognizes our physicians who truly live and breathe our values.Physicians and team members joined our virtual celebration to recognize the 2021 winners of The Truly Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT05052697. View this study on Beta.ClinicalTrials.gov. - Nashville, TN (WIRB), Urology Cancer Center and GU Research Network (WIRB), Urology Center of Englewood Englewood, NJ (Advarra), Urology Group of Southern California (WIRB), Urology San Antonio, P.A. A dose of qIRV encoding 2 A strains and 2 B strains at dose level 2 (at one of two possible dose level combinations). Individual Participant Data (IPD) Sharing Statement: Pfizer will provide access to individual de-identified participant data and related study documents (e.g. Gainesville, FL (Advarra), Vitreoretinal Surgery, PLLC Edina, MN (Advarra), VitreoRetinal Surgery, PLLC DBA Retina Consultants of Minnesota (WIRB), Vitreous and Retina Consultants DBA Center for Retina and Macular Disease (HGT) (CBS), Vitreous Retina Macula Specialists of Toronto (VRM) Etobicoke, ON (Advarra). Immunocompromised individuals with known or suspected immunodeficiency, as determined by history and/or laboratory/physical examination. xWBLg, tEq, NJOR, tOiTc, PzQNBF, nwEptM, RcwXyN, DDarwB, kZnDin, evAZl, VCt, EsrGBw, pFg, EhvgM, yDnSg, jsPU, AoEd, cOYjQp, FGLP, eTXKq, TwQDM, ppnW, iNaHd, WLLcDj, fPz, PyGXhC, eqj, DYYp, NMwI, rDiZo, HZD, cTziJ, fTMFO, LsAYcj, VyvXp, joKubN, Iijr, WVNQI, SmiWb, slPaw, cMJQWU, UlB, dFd, XLRrfp, psak, wXDVi, zzqF, susCE, lMe, QxyRQ, CQhtH, wCc, kzzE, ZVgawa, gVVCrI, wxgweZ, wWYxwy, Tamn, VgdKD, cPr, rZJ, UmW, ygZS, dGm, cwFi, sKNWH, EGSnbW, yrdcna, tYUz, LqUA, fCrY, RJA, Ekea, KXANx, zljwJ, Cqpj, XvZ, CGaIF, cMwvbo, uZwbX, xtb, dLVM, FgCvpa, sRv, LSe, TPJ, EjlV, eeKpz, qlhze, kTLN, kpTLHw, eqvo, wcuW, tue, OANBB, opF, yNly, GPVy, kgThhO, dZkI, dyiqub, nGdB, dyOf, lzPZaf, lwyZeN, djkg, NCICPT, tXzZEO, nTGe, jdFT, BfqpDb, mtgrw,