Individual Participant Data (IPD) Sharing Statement: Studies a U.S. FDA-regulated Drug Product: Studies a U.S. FDA-regulated Device Product: Occurrence of LRTD [TimeFrame:Over one RSV season (at least 6 months, and up to 12 months post vaccination)], Occurrence of ARD [TimeFrame:Over one RSV season (at least 6 months, and up to 12 months post vaccination)], Occurrence of complications and hospitalizations [TimeFrame:Over one RSV season (at least 6 months, and up to 12 months post vaccination)], Occurrence of any serious adverse events [TimeFrame:Up to 24 months after vaccination], Occurrence of any grade 3 or higher adverse events [TimeFrame:Within 29 days after vaccination], Occurrence of solicited local adverse events [TimeFrame:Within 8 days after vaccination], Occurrence of solicited systemic adverse events [TimeFrame:Within 8 days after vaccination], Occurrence of any unsolicited adverse events [TimeFrame:Within 29 days after vaccination], RSV-specific T-cell responses [TimeFrame:Within 1 week after vaccination], RSV-specific serum IgG antibody titers [TimeFrame:2 weeks after vaccination], RSV-specific serum neutralizing antibody titers [TimeFrame:Within 2 weeks after vaccination]. WebTidewater Physicians Multispecialty Group includes over 200 family medicine and specialty physicians, including advanced practice providers. 152 19028447 152537 151979 0.94035545474212812 0.94082077129077046 2.9468260159830072e-2 Communicate with your TPMG provider, receive test results and request in-person and telemedicine appointments through our Patient Portal. What do you do if you miss an appointment, cancel or need to reschedule an appointment at a TPMG office? View this study on Beta.ClinicalTrials.gov. WebSuffolk Multispecialty Research (CBS) Sugar Lakes Family Practice Sugar Land, TX (Advarra) Summa Health (WIRB) Summit Headlands, LLC Portland, OR (Advarra) Summit Medical Group (WIRB) Summit Medical Group P.A. Dr. Kerry McGregor, PsyD also suggests that some children express their gender identity as soon as they can talk. Studies a U.S. FDA-regulated Drug Product: Studies a U.S. FDA-regulated Device Product: Number of first episode of RSV-associated lower respiratory tract illness (LRTI-RSV) in the first RSV season [TimeFrame:From Day 15 after vaccination until the end of season 1 visit (an average of 6 months)], Proportion of participants reporting prompted local reactions within 7-days after vaccination [TimeFrame:Within 7 days after vaccination], Proportion of participants reporting prompted systemic events within 7-days after vaccination [TimeFrame:Within 7 days after vaccination], Proportion of participants reporting AE within 1-month after vaccination [TimeFrame:Within 1 month after vaccination (up to 35 days)], Proportion of participants reporting SAE throughout the study [TimeFrame:Throughout the study duration (an average of 30 months)], Proportion of participants reporting NDCMC throughout the study [TimeFrame:Throughout the study duration (an average of 30 months)], Number of first episode of RSV-associated severe LRTI (sLRTI-RSV) in the first RSV season [TimeFrame:From Day 15 after vaccination until the end of season 1 visit (an average of 6 months)], Number of first episode of LRTI-RSV in the second RSV season [TimeFrame:During the second RSV season (an average of 6 months)], Number of first episode of LRTI-RSV across 2 RSV seasons [TimeFrame:From Day 15 after vaccination until the end of season 2 visit (an average of 12 months of surveillance)], Number of first episode of RSV-associated ARI (ARI-RSV) in the first RSV season [TimeFrame:From Day 15 after vaccination until the end of season 1 visit (an average of 6 months)], Number of first episode of ARI-RSV in the second RSV season [TimeFrame:During the second RSV season (an average of 6 months)], Number of first episode of ARI-RSV across 2 RSV seasons [TimeFrame:From Day 15 after vaccination until the end of season 2 visit (an average of 12 months of surveillance)], Number of first episode of sLRTI-RSV in the second RSV season [TimeFrame:During the second RSV season (an average of 6 months)], Number of first episode of sLRTI-RSV across 2 RSV seasons [TimeFrame:From Day 15 after vaccination until the end of season 2 visit (an average of 12 months of surveillance)], Respiratory Syncytial Virus Subgroup A (RSV A) and RSV B neutralizing titers [TimeFrame:Before vaccination, 1-month after vaccination, before season 2 (approximately 12 months after vaccination)]. WebWe would like to show you a description here but the site wont allow us. History of allergic disease or reactions likely to be exacerbated by any component of the vaccine, e.g., tris(hydroxymethyl)-amino methane, chicken embryo fibroblast proteins, gentamycin, ciprofloxacin; this includes: Any administration or planned administration of: To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor. Our physicians have long-standing relationships with the patients they serve and are well respected for their medical and community leadership. Choosing to participate in a study is an important personal decision. Individual Participant Data (IPD) Sharing Statement: Pfizer will provide access to individual de-identified participant data and related study documents (e.g. - Vega Baja (WIRB), West Coast Research LLC Dublin, CA (Advarra), West Coast Retina Medical Group, Inc. (WIRB), West Houston Clinical Research Service Houston, TX (Advarra), West Houston Clinical Research Service, LLC (WIRB), West Michigan Clinical Research Center Wyoming, MI (Advarra), West Virginia Research Institute PLLC (WIRB), West Virginia School of Osteopathic Medicine, West Virginia University Eye Institute Morgantown, WV (Advarra), Western Carolina Retinal Associates P.A. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. Call 646-929-7800 or Redness and swelling were measured and recorded in measuring device units. Occurrence of LRTD associated with RSV until the end of one RSV season (at least 6 months, and up to 12 months post vaccination). 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. Vomiting was graded as mild: 1 to 2 times in 24 hours(h), moderate: >2 times in 24h and severe: requires intravenous hydration. For participants 65 to 85 years of age at the time of enrollment, receipt of licensed influenza vaccination for the 2021-2022 northern hemisphere season >4 months (120 days) before study intervention administration. There are many treatments available to reduce or eliminate pain in the neck. Bleeding diathesis or condition associated with prolonged bleeding that would, in the opinion of the investigator, contraindicate intramuscular injection. Testing methods and laboratory result interpretation techniques are also studied extensively. The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Use of any investigational or non-registered drug or vaccine other than the trial vaccine within 30 days prior to the administration of the trial vaccine, or planned administration of such a drug or vaccine between enrollment in the trial and until 4 weeks after the trial vaccine administration. Substudy A This is a Phase 1 randomized substudy to evaluate the safety and immunogenicity of monovalent influenza modRNA vaccine (mIRV) and bivalent influenza modRNA vaccine (bIRV) at various dose levels, and quadrivalent influenza modRNA vaccine (qIRV), in participants 65 to 85 years of age. Active or recent (within 6 months before enrollment) history of chronic alcohol abuse. Occurrence of complications and hospitalizations related to PCR-confirmed RSV disease. 1 measuring device unit =0.5 cm and graded as mild: 2.5 to 5.0 cm, moderate: > 5.0 to 10.0 cm and severe: >10 cm. LRTI-RSV is defined as an ARI with 2 or more of the lower respiratory signs/symptoms lasting more than 1 day during the same illness, plus RT-PCR-confirmed RSV infection within 7 days of ARI symptom onset. ; Texas Oncology Cancer Center- Abilene, TX (WIRB), Texas Oncology, PA (Austin, Midtown) (WIRB), Texas Oncology-Medical City (Txo-MC) (USOR) (CBS), Texas Oncology-Sammons Cancer Center (WIRB), Texas Oncology-San Antonio (Txo-SA) (CBS), Texas Orthopedic Specialists, PLLC Bedford, TX (Advarra), Texas Retina Associates Arlington, TX (Advarra), Texas Retina Associates Dallas, TX (Advarra), Texas Retina Associates Plano, TX (Advarra), Texas State University, (TSU) -San Marcos, Texas Tech University Health Sciences Center El Paso, Texas Tech University, Health Sciences Center (TTUHS), The Arthritis and Diabetes Clinic Monroe, LA (Advarra), The Center for Diabetes and Endocrine Care (ADVARRA), The Center for Rheumatology and Bone Research (ADVARRA), The Childrens Clinic of Jonesboro, P.A. Microsoft pleaded for its deal on the day of the Phase 2 decision last month, but now the gloves are well and truly off. 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. Web7/1/2022 7/1/2022 7/1/2022 6/26/2022 7/1/2022 6/26/2022 7/1/2022 6/26/2022. SSA: Percentage of participants reporting local reactions [TimeFrame:For 7 days after Vaccinations 1 and 2], SSA: Percentage of participants reporting systemic events [TimeFrame:For 7 days after Vaccinations 1 and 2], SSA: Percentage of participants reporting adverse events [TimeFrame:From vaccination to 4 weeks after Vaccinations 1 and 2], SSA: Percentage of participants reporting serious adverse events [TimeFrame:From vaccination to 6 months after the last study vaccination], SSA: Percentage of participants with abnormal hematology and chemistry laboratory values [TimeFrame:2 days after Vaccination 1], SSA: Percentage of participants with abnormal hematology and chemistry laboratory values [TimeFrame:1 week after Vaccination 1], SSA: Percentage of participants with grading shifts in hematology and chemistry laboratory assessments [TimeFrame:Between baseline and 2 days after Vaccination 1], SSA: Percentage of participants with grading shifts in hematology and chemistry laboratory assessments [TimeFrame:Between baseline and 1 week after Vaccination 1], SSA: Percentage of participants with new electrocardiogram (ECG) abnormalities [TimeFrame:2 days after Vaccination 1], SSA: Percentage of participants with new ECG abnormalities [TimeFrame:1 week after Vaccination 1], SSB: Percentage of participants reporting local reactions (18 to 64 and 65 to 85 years of age) [TimeFrame:For 7 days after each vaccination], SSB: Percentage of participants reporting systemic events (18 to 64 and 65 to 85 years of age) [TimeFrame:For 7 days after each vaccination], SSB: Percentage of participants reporting adverse events (18 to 64 and 65 to 85 years of age) [TimeFrame:From Vaccination 1 to 4 weeks after the last vaccination], SSB: Percentage of participants reporting serious adverse events (18 to 64 and 65 to 85 years of age) [TimeFrame:From Vaccination 1 to 6 months after the last vaccination], SSB: Percentage of participants with abnormal troponin I laboratory values (18 to 64 and 65 to 85 years of age) [TimeFrame:2 days after the last vaccination], SSB: Percentage of participants with new ECG abnormalities (18 to 64 and 65 to 85 years of age) [TimeFrame:2 days after the last vaccination], SSA: Geometric mean titers (GMTs) of hemagglutination inhibition (HAI) titers [TimeFrame:At Baseline, and 1-, 4- and 8-weeks after Vaccination 1], SSA: Geometric mean fold rise (GMFR) in HAI titers from before vaccination to each subsequent timepoint [TimeFrame:At 1-, 4-, and 8-weeks after Vaccination 1], SSA: Proportion of participants achieving HAI seroconversion for each strain [TimeFrame:At 1-, 4-, and 8-weeks after Vaccination 1], SSA: Proportion of participants with HAI titer >=1:40 for each strain [TimeFrame:At Baseline, and 1-, 4-, and 8-weeks after Vaccination 1], SSA: In participants who receive either qIRV or QIV at Vaccination 1, the proportion of participants achieving HAI seroconversion for all strains [TimeFrame:At 1-, 4-, and 8-weeks after Vaccination 1], SSA: In participants who receive either qIRV or QIV at Vaccination 1, the proportion of participants with HAI titer >=1:40 for all strains [TimeFrame:At Baseline, and 1-, 4-, and 8-weeks after Vaccination 1], SSA: The geometric mean ratio (GMR) of the geometric mean of HAI titers from participants receiving qIRV to the geometric mean of HAI titers from participants receiving QIV [TimeFrame:At 4 weeks after Vaccination 1], SSA: The difference in percentage of participants achieving HAI seroconversion for each strain in qIRV recipients compared to licensed QIV recipients [TimeFrame:At 4 week after Vaccination 1], SSB: GMTs of HAI titers (65-85 years of age) [TimeFrame:At Baseline, prior to Vaccination 2 (if applicable), and 1-, 4- and 8-weeks after the last vaccination], SSB: GMFR in HAI titers from before vaccination to each subsequent timepoint (65-85 years of age) [TimeFrame:Prior to Vaccination 2 (if applicable), and at 1-, 4-, and 8-weeks after the last vaccination], SSB: Proportion of participants achieving HAI seroconversion for each strain (65-85 years of age) [TimeFrame:Prior to Vaccination 2 (if applicable), and at 1-, 4-, and 8-weeks after the last vaccination], SSB: Proportion of participants with HAI titer >=1:40 for each strain (65-85 years of age) [TimeFrame:At Baseline, prior to Vaccination 2 (if applicable), and 1-, 4-, and 8-weeks after the last vaccination], SSB: In participants who receive either qIRV or QIV, the proportion of participants achieving HAI seroconversion for all strains (65-85 years of age) [TimeFrame:Prior to Vaccination 2 (if applicable), and at 1-, 4-, and 8-weeks after the last vaccination], SSB: In participants who receive either qIRV or QIV at Vaccination 1, the proportion of participants with HAI titer >=1:40 for all strains (65-85 years of age) [TimeFrame:At Baseline, prior to Vaccination 2 (if applicable), and 1-, 4-, and 8-weeks after the last vaccination], SSB: GMTs of HAI titers (18-64 years of age) [TimeFrame:At Baseline, prior to Vaccination and 1-, 4- and 8-weeks after vaccination], SSB: GMFR in HAI titers from before vaccination to each subsequent timepoint (18-64years of age) [TimeFrame:Prior to Vaccination, and at 1-, 4-, and 8-weeks after vaccination], SSB: Proportion of participants achieving HAI seroconversion for each strain (18-64 years of age) [TimeFrame:Prior to Vaccination, and at 1-, 4-, and 8-weeks after vaccination], SSB: Proportion of participants with HAI titer >=1:40 for each strain (18-64 years of age) [TimeFrame:At Baseline, prior to Vaccination, and 1-, 4-, and 8-weeks after vaccination], SSB: In participants who receive either qIRV or QIV, the proportion of participants achieving HAI seroconversion for all strains (18-64 years of age) [TimeFrame:Prior to Vaccination, and at 1-, 4-, and 8-weeks after vaccination], SSB: In participants who receive either qIRV or QIV at Vaccination 1, the proportion of participants with HAI titer >=1:40 for all strains (18-64 years of age) [TimeFrame:At Baseline, prior to Vaccination, and 1-, 4-, and 8-weeks after vaccination]. WebEarn your nursing degree in as little as 36 months, by enrolling in our Bachelor of Science in Nursing (BSN) program. Reverse Transcriptase-Polymerase Chain Reaction (RT-PCR)-confirmed RSV A and/or RSV B- associated acute respiratory illness (ARI) is assessed. Informed Consent signed by the subject. WebEarn your nursing degree in as little as 36 months, by enrolling in our Bachelor of Science in Nursing (BSN) program. 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. 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 heart failure (CHF), hypertension, type 2 diabetes mellitus, hyperlipoproteinemia, or hypothyroidism, that is clinically stable as assessed by the investigator. Allergy to egg proteins (egg or egg products) or chicken proteins. These steps will take your soup recipe to the next level. This was a promotional video for the hospital. By offering a long list of benefits, as well as ample opportunities for career advancement, TPMG understands if we take care of our employees, our employees will have the ability to continue to enforce our mission and provide the best care to our patients. Talk with your doctor and family members or friends about deciding to join a study. Specific criteria for participants with known stable infection with HIV, HCV, or HBV can be found in the protocol. Any participant who has received or plans to receive a modRNA-platform SARS-CoV-2 vaccine within 60 days of Visit 1. This was a promotional video for the hospital. Since our BSN program offers an accelerated year-round schedule, our graduates can complete their nursing school requirements and enter the workforce sooner than if they were to attend a traditional four-year college.Surgical Technologist One injection, solution for injection, intramuscular use, 0.5mL TBS, pH 7.7. Multispecialty group practice: $223,000; Single specialty group practice: $188,00; Solo practice: $225,000 Suffolk Massachusetts. You might have plantar fasciitis. An NDCMC is defined as a disease or medical condition, not previously identified, that is expected to be persistent or otherwise long-lasting in its effects (eg, asthma). Choosing to participate in a study is an important personal decision. 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. What do you do if you miss an appointment, cancel or need to reschedule an appointment at a TPMG office? To obtain contact information for a study center near you, click here. Web< 1 min. Today, TPMG has expanded its practices to include over 220 primary care, specialty physicians, and advanced practice clinicians who Choosing to participate in a study is an important personal decision. 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. Ctr. (HGT) (CBS), Western Michigan University Homer Stryker MD School of Medicine, Western New York Urology Associates (Advarra), Western Regional Medical Center, dba CTCA Phoenix (WIRB), Westside Center for Clinical Research (CBS), Westside Center for Clinical Research Jacksonville, FL (Advarra), Whitehead Institute for Biomedical Research, Willamette Valley Cancer Institute & Research Center (ADVARRA), Willamette Valley Cancer Institute and Research Center (CBS), William Beaumont Hospital Research Institute, Wilmington Health Wilmington, NC (Advarra), Wolfe Clinic, PC (dba Wolfe Eye Clinic) (CBS), Women Under Study, LLC New Orleans, LA (Advarra, Women's Cancer Care Associates, LLC (WIRB), Womens Cancer Research Network (WCRN)/COGI Fresno, CA (Advarra), Womens Partners in Health, PLLC Austin, TX (Advarra), Woodland International Research Group, LLC Little Rock, AR (Advarra), WR-ClinSearch Chattanooga, TN (Advarra), WR-Global Medical Research, LLC (Advarra), WR-Mount Vernon Clinical Research, LLC Sandy Springs, GA (Advarra), WR-Pharmacology Research Institute Los Alamitos, CA (Advarra), WR-Pharmacology Research Institute Newport Beach, CA (Advarra), Wroclawskie Centrum Zdrowia SP ZOZ (WIRB), Wyss Institute for Biologically Inspired Engineering at Harvard University, XCANCER / Tennessee Cancer Specialists (CBS), Zenos Clinical Research, LLC Dallas, TX (Advarra). protocol, Statistical Analysis Plan (SAP), Clinical Study Report (CSR)) upon request from qualified researchers, and subject to certain criteria, conditions, and exceptions. 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. Individuals who receive chronic systemic treatment with immunosuppressive therapy, including cytotoxic agents, monoclonal antibodies, systemic corticosteroids, or radiotherapy, eg, for cancer or an autoimmune disease, from 60 days before study intervention administration or planned receipt throughout the study. Occurrence of any serious adverse events at any time during the trial period. 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. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. Local reactions included pain at injection site, redness and swelling recorded by participants in an e-diary. WebWe would like to show you a description here but the site wont allow us. The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Individual Participant Data (IPD) Sharing Statement: Pfizer will provide access to individual de-identified participant data and related study documents (e.g. Participants may be enrolled in either the reactogenicity subset, immunogenicity subset, or both subsets. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Are you looking for a healthier diet to kickstart the new year? (WIRB), Center for Rare Neurological Diseases (CBS), Center for Retina and Macular Disease (ADVARRA), Centers for Disease Control/National Center for Infectious Diseases CDC/NCID, Centex Studies Lake Charles, LA (Advarra), Centex Studies, Inc. Lake Charles (CBS), Central Arizona Medical Associates Mesa, AZ (Advarra), Central Maine Medical Center Hematology & Oncology (Advarra), Central Michigan University - Detroit (WIRB), Central Phoenix Medical Clinic, LLC / Synexus Clinical Research US, Inc. HGT (CBS), Central Research Associates, Inc. HGT (Advarra), Central Valley Research Modesto, CA (Advarra), Centre de Recherche Saint-Louis - Quebec, QC (Advarra), Centricity Research Columbus, GA (Advarra), Centricity Research Columbus Ohio Multispecialty (WIRB), Centricity Research Phoenix Multispecialty (WIRB), Centricity Research Suffolk Primary Care Suffolk, VA (Advarra), Centro de Atencion y Diagnostico de Enfermedades Infecciosas S.A. (CDI SA) (WIRB), Centro de Estudos e Pesquisas em Molestias Infecciosas - LTDA (WIRB), Centro de Investigaciones Technologicas Biomedicas (CITBM) Y Medioambientales and Unidad de Ensayos Clinicos (UNIDEC) (WIRB), Centro de Pesquisas Clinicas do Hospital das Clinicas da UFMG (WIRB), Centro de Referncia e Treinamento DST/AIDS, Centro de Referencia e Treinamento DST/AIDS (WIRB), Centro de Referencia Professor Helio Fraga (CRPHF/ENSP/FIOCRUZ) (WIRB), Centura Health Centennial, CO (Advarra), Centura Health, Avista Adventist Hospital Louisville, CO (Advarra), Centura Health, Littleton Adventist Hospital Littleton, CO (Advarra), Centura Health, Mercy Regional Medical Center Durango, CO (Advarra), Centura Health, Parker Adventist Hospital Parker, CO (Advarra), Centura Health, Penrose Hospital Colorado Springs, CO (Advarra), Centura Health, Porter Adventist Hospital Denver, CO (Advarra), Centura Health, St. Anthony Hospital Lakewood, CO (Advarra), Centura Health, St. Anthony North Campus Westminster, CO (Advarra), Centura Health, St. Francis Medical Center Colorado Springs, CO (Advarra), Certified Foot & Ankle Specialists Boca Raton, FL (Advarra), Certified Foot & Ankle Specialists, LLC St. Petersburg, FL (Advarra), Chan Soon-Shiong Institute for Medicine (Advarra), Chandler Clinical Trials, LLC Chandler, AZ (Advarra), Charles R. Drew University of Medicine and Science, Charles R. Drew University of Medicine and Science Los Angeles, CA (Advarra), Charles Retina Institute Germantown, TN (Advarra), Charleston Neuroscience Institute, LLC - Beaufort (CBS), Charleston Neuroscience Institute, LLC Beaufort, SC (Advarra), Charleston Neuroscience Institute, LLC Ladson, SC (Advarra), Charleston Neuroscience Institute, LLC, West Ashley Charleston, SC (Advarra), Charlottesville Medical Research Center, LLC Charlottesville, VA (Advarra), Chase Medical Research Waterbury, CT (Advarra), Chattanooga Medical Research, LLC (WIRB), Chattanooga Medical Research, LLC Chattanooga, TN (Advarra), Chattanooga's Program in Women's Oncology (WIRB), Chemidox Clinical Trials, Inc. Lancaster, CA (Advarra), Cherry Health Grand Rapids, MI (Advarra), Chesapeake Urology Associates, LLC d/b/a/ Chesapeake Urology Research Associates (CBS), Chesapeake Urology Research Associates (WIRB), Chesapeake Urology Research Associates - Hanover (WIRB), Chesapeake Urology Research Associates Baltimore, MD (Advarra), Chesapeake Urology Research Associates Hanover, MD (Advarra), CHI Franciscan Health, St Joseph Medical Center (ADVARRA), Chicago Association for Research and Education in Science (CARES), Chicago Clinical Research Institute Chicago, IL (Advarra), Children's Cancer Therapy Development Institute, Children's Healthcare of Atlanta, Inc. (WIRB), Children's Hospital of Orange County (WIRB), Children's Hospital of Philadelphia Research Institute, Children's Hospital of Wisconsin/Medical College of Wisconsin, (MCW), Children's National Research Institute of Children's National Medical (WIRB), Childrens Hospital Los Angeles Los Angeles, CA (Advarra), Childrens Hospital of Eastern Ontario Research Institute, Inc. Ottawa, ON (Advarra), Childrens Hospital of Los Angeles (CHLA) (CBS), Childrens Hospital of Orange County (CHOC) (CBS), Childrens Hospital of Orange County (CHOC) Orange, CA (Advarra), Childrens Hospital of The Kings Daughters Norfolk, VA (Advarra), Childrens Hospital of The Kings Daughters HGT (CBS), Chow Berger Koushan Medical Professional Corporation (CBS), Christie Clinic Champaign, IL (Advarra), Christina Care Health Systems/Thomas Jefferson University, Christina Sebestyen, MD, PA dba OBGYN North Austin, TX (Advarra), CHRISTUS Institute for Innovation and Advanced Clinical Care (WIRB), Cincinnati Children's Hospital Medical Center, Circuit Clinical West Seneca, NY (Advarra), Circuit Clinical/Alliance Health Center Jersey City, NJ (Advarra), Circuit Clinical/David Avino, MD, PC Orchard Park, NY(Advarra), Circuit Clinical/Hamburg Regional Gynecology Group Orchard Park, NY (Advarra), Circuit Clinical/Invision Williamsville, NY (Advarra), Circuit Clinical/IZ Medical Center - Moonachie, NJ (Advarra), Circuit Clinical/OB.GYN Associates of NY West Seneca, NY (Advarra), Circuit Clinical/Orchard Park Family Practice, PC Orchard Park, NY (Advarra), Circuit Clinical/Riverside Medical Group - Secaucus, NJ (Advarra), Circuit Clinical/Urban Family Practice Buffalo, NY (Advarra), City University of New York, Advanced Science Research Center (CUNY ASRC), City University of New York, College of Staten Island, City University of New York, Lehman College, (CUNYLC), City University of New York, Queens College, (CUNYQC), Cleveland Clinic Florida Research & Innovation Center, Clinic for Special Children Strasburg, PA (Advarra), Clinica Especializada Condesa-Iztapalapa "Dr. Jaime Sepulveda Amor" (CECI) (WIRB), Clinical Alliance for Research & Education - Infectious Diseases (WIRB), Clinical Investigations, LLC Edmond, OK (Advarra), Clinical Neuroscience Solutions, Inc. (WIRB), Clinical Neuroscience Solutions, Inc. - Jacksonville (WIRB), Clinical Neuroscience Solutions, Inc. - Memphis (WIRB), Clinical Research Associates Cortland, NY (Advarra), Clinical Research Associates, Inc. Nashville, TN (Advarra), Clinical Research Associates, LLC Huntsville, AL (Advarra), Clinical Research Atlanta Stockbridge, GA (Advarra), Clinical Research Center of Alabama (dba Allervie Clinical Research) Birmingham, AL (Advarra), Clinical Research Center of Florida Pompano Beach, FL (Advarra), Clinical Research Center of Reading, LLC (ADVARRA), Clinical Research Center of the Carolinas Charleston, SC (Advarra), Clinical Research Consortium - Nevada (WIRB), Clinical Research Consulting, LLC Milford, CT (Advarra), Clinical Research Institute, Inc. (Advarra), Clinical Research Institute, Inc. Minneapolis, MN (Advarra), Clinical Research of Gastonia Gastonia, NC (Advarra), Clinical Research of South Nevada Las Vegas, NV (Advarra), Clinical Research of West Florida HGT (Advarra), Clinical Research of West Florida, Inc. (WIRB), Clinical Research Professionals Chesterfield, MO (Advarra), Clinical Research Professionals, LLC (CBS), Clinical Research Professionals, LLC (WIRB), Clinical Research Puerto Rico - Guayama (WIRB), Clinical Research Puerto Rico San Juan, PR (Advarra), Clinical Research Solutions Jackson, TN (Advarra), Clinical Research Solutions Middleburg Heights, OH (Advarra), Clinical Research Trials of Florida, Inc. (WIRB), Clinical Research Trials of Florida, Inc. Tampa, FL (Advarra), Clinical Site Partners Winter Park, FL (Advarra), Clinical Site Partners LLC d/b/a CSP-Leesburg (CBS), Clinical Site Partners LLC d/b/a CSP-Miami (CBS), Clinical Site Partners, LLC Miami, FL (Advarra), Clinical Site Partners, LLC d/b/a CSP-Orlando (CBS), Clinical Trials Managements, LLC Metairie, LA (Advarra), Clinical Trials of America, LLC Hickory, NC (Advarra), Clinical Trials of America, LLC Monroe, LA (Advarra), Clinical Trials of America, LLC Mt. Except Bilirubin, other stable Grade1 abnormalities may be considered eligible by Investigator. Copyright Tidewater Physicians Multispecialty Group, Tidewater Accountable Care Organization, LLC, Plant-Based Dieting: A Tasty Way to Eat Healthy, Joint Pain In The Neck: Recognize the Signs and Find Treatment, RSV on the Rise: What You Need To Know To Keep Your Children Safe, Wearing Ear Plugs to Your Next Concert Might Save Your Hearing, Make Face Washing a Priority for Clearer, Healthier Skin, Making Your Favorite Fall Soup Recipes Healthy and Filling, Walking Through Fire: Plantar Fasciitis Symptoms and Treatment, Orthopedics | Spine | Sports Medicine | Foot and Ankle | Hand, Why You Should Get a Flu Shot This Year (And Every Year), TPMG is Decorating Bras for Breast Cancer. Family medicine is a branch of primary care that acts in a generalist function to provide personal, front-line medical care to patients. 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. By offering a long list of benefits, as well as ample opportunities for career advancement, TPMG Since our BSN program offers an accelerated year-round schedule, our graduates can complete their nursing school requirements and enter the workforce sooner than if they were to attend a traditional four-year college.Surgical Technologist WebIt is Northwell Healths policy to provide equal employment opportunity and treat all applicants and employees equally regardless of their age, race, creed/religion, color, national origin, immigration status or citizenship status, sexual orientation, military or veteran status, sex/gender, gender identity, gender expression, disability, pregnancy, genetic 75/Sherman TX (Advarra), CardioVoyage 4510 Med. Participants will receive at Vaccination 1 either: At approximately 8 weeks following Vaccination 1, participants will be unblinded and QIV (Vaccination 2) administered to participants not having previously received this at Vaccination 1. Communicate with your TPMG provider, receive test results and request in-person and telemedicine appointments through our Patient Portal. Vaccination with any investigational or licensed influenza vaccine within 6 months (175 days) before study intervention administration. https://www.pfizer.com/science/clinical_trials/trial_data_and_results/data_requests. 1 dose of licensed QIV (as a control group). Inclusion Criteria: Male and female subjects 60 years of age. If systemic corticosteroids have been administered short term (<14 days) for treatment of an acute illness, participants should not be enrolled in the study until corticosteroid therapy has been discontinued for at least 28 days before study intervention administration. Participants who are willing and able to comply with all scheduled visits, vaccination plan, laboratory tests, lifestyle considerations, frequent symptom assessment by mobile device application, and other study procedures, including collection of nasal swabs by themselves and by study staff when indicated. ClinicalTrials.gov Identifier: NCT05238025, Interventional Testing methods and laboratory result interpretation techniques are also studied extensively. WebSearch Education & Research. Study record managers: refer to the Data Element Definitions if submitting registration or results information. St. Vincent Hospital and Health Care Center, Inc. St. Vincents Health System Birmingham, AL (Advarra), State University of New York (SUNY) Polytechnic Institute, State University of New York (SUNY) Upstate Medical University, State University of New York, (SUNY) Albany, State University of New York, (SUNY) Binghamton, State University of New York, (SUNY) Brockport, State University of New York, (SUNY) Stony Brook, Steadman Philippon Research Institute, Fort Collins (WIRB), Steadman Philippon Research Institute, Vail (WIRB), Stedman Clinical Trials Tampa, FL (Advarra), Sterling Research Group Auburn Ave, Cincinnati (CBS), Sterling Research Group Glensprings Dr, Cincinnati (CBS), Sugar Lakes Family Practice Sugar Land, TX (Advarra), Summit Headlands, LLC Portland, OR (Advarra), Sun Research Institute San Antonio, TX (Advarra), Sunbeam Clinical Research 10640 Riverside Dr, Fort Worth, TX (Advarra), Sunbeam Clinical Research 1325 Pennsylvania Ave, Fort Worth, TX (Advarra), Sunbeam Clinical Research 4004 Medical Pkwy/Greenville, TX (Advarra), Sunbeam Clinical Research 403 Campbell Rd, Richardson, TX (Advarra), Sunbeam Clinical Research 409 Ridgecrest Rd/Greenville, TX (Advarra), Sunbeam Clinical Research Grapevine, TX (Advarra), Sunbeam Clinical Research Lewisville, TX (Advarra), Sunbeam Clinical Research McKinney, TX (Advarra), Sunbeam Clinical Research Sherman, TX (Advarra), Sunbright Health Medical Center Homestead, FL (Advarra), Suncoast Clinical Research, Inc. New Port Richey, FL (Advarra), Suncoast Research North Miami Beach (CBS), Suncoast Research Associates - Hallandale (CBS), Suncoast Research Associates Miami (CBS), Suncoast Research Associates Miami Lakes (CBS), Suncoast Research Associates, LLC Miami, FL (Advarra), Suncoast Research Group, LLC Miami, FL (Advarra), Sundance Clinical Research, LLC HGT (CBS), Sunrise Research Institute Sunrise, FL (Advarra), SUNY Upstate Medical University Syracuse, NY (Advarra, Sutter Valley Hospitals d/b/a Sutter Institute for Medical Research (ADVARRA), Sweet Hope Research Specialty, Inc. Hialeah, FL (Advarra), Synexus Clinical Research The Villages, FL (Advarra), Synexus Clinical Research US, Inc Anderson, SC (Advarra - HGT), Synexus Clinical Research US, Inc Phoenix, AZ (Advarra - HGT), Synexus Clinical Research US, Inc. - Chicago (CBS), Synexus Clinical Research US, Inc. - Colorado Springs (CBS), Synexus Clinical Research US, Inc. - Dallas (CBS), Synexus Clinical Research US, Inc. - Phoenix Southeast (CBS), Synexus Clinical Research US, Inc. - San Antonio (CBS), Synexus Clinical Research US, Inc. - St. Petersburg (CBS), Synexus Clinical Research US, Inc. - The Villages (CBS), Synexus Clinical Research US, Inc. -New York (CBS), Synexus Clinical Research US, Inc. E. Southern Ave, Mesa (CBS), Synexus Clinical Research US, Inc. Layton (CBS), Synexus Clinical Research US, Inc. Akron, OH (Advarra), Synexus Clinical Research US, Inc. Akron, OH HGT (CBS), Synexus Clinical Research US, Inc. Anderson (CBS), Synexus Clinical Research US, Inc. Anderson, SC (Advarra), Synexus Clinical Research US, Inc. Atlanta (CBS), Synexus Clinical Research US, Inc. Atlanta, GA (Advarra), Synexus Clinical Research US, Inc. Birmingham (CBS), Synexus Clinical Research US, Inc. Birmingham, AL (Advarra), Synexus Clinical Research US, Inc. Centennial (CBS), Synexus Clinical Research US, Inc. Centennial, CO (Advarra), Synexus Clinical Research US, Inc. Cerritos (CBS), Synexus Clinical Research US, Inc. Cerritos, CA (Advarra), Synexus Clinical Research US, Inc. Chandler, AZ (Advarra), Synexus Clinical Research US, Inc. Chicago, IL (Advarra), Synexus Clinical Research US, Inc. Cincinnati, OH (Advarra), Synexus Clinical Research US, Inc. Cincinnati, OH HGT (CBS), Synexus Clinical Research US, Inc. Colorado Springs, CO (Advarra), Synexus Clinical Research US, Inc. Columbus (CBS), Synexus Clinical Research US, Inc. Columbus, OH (Advarra), Synexus Clinical Research US, Inc. Dallas, TX (Advarra), Synexus Clinical Research US, Inc. E Greenville Street, Anderson (CBS), Synexus Clinical Research US, Inc. East Brown Rd, Mesa (CBS), Synexus Clinical Research US, Inc. Evansville, IN HGT (CBS), Synexus Clinical Research US, Inc. Evansville, IN (Advarra), Synexus Clinical Research US, Inc. Glendale, AZ (Advarra), Synexus Clinical Research US, Inc. Glendale, AZ (CBS), Synexus Clinical Research US, Inc. Greer (CBS), Synexus Clinical Research US, Inc. Henderson (CBS), Synexus Clinical Research US, Inc. Henderson, NV (Advarra), Synexus Clinical Research US, Inc. Jamaica, NY (Advarra), Synexus Clinical Research US, Inc. Layton, UT (Advarra), Synexus Clinical Research US, Inc. Mesa, AZ (Advarra), Synexus Clinical Research US, Inc. Murray, UT (Advarra), Synexus Clinical Research US, Inc. Murray, UT HGT (CBS), Synexus Clinical Research US, Inc. New York, NY (Advarra), Synexus Clinical Research US, Inc. Oklahoma City (CBS), Synexus Clinical Research US, Inc. Oklahoma City, OK (Advarra), Synexus Clinical Research US, Inc. Omaha, NE (Advarra), Synexus Clinical Research US, Inc. Omaha, NE HGT (CBS), Synexus Clinical Research US, Inc. Orlando (CBS), Synexus Clinical Research US, Inc. Orlando, FL (Advarra), Synexus Clinical Research US, Inc. Papillion (CBS), Synexus Clinical Research US, Inc. Papillion, NE (Advarra), Synexus Clinical Research US, Inc. Phoenix Central (CBS), Synexus Clinical Research US, Inc. Phoenix, AZ (Advarra), Synexus Clinical Research US, Inc. Pinellas Park, FL (Advarra), Synexus Clinical Research US, Inc. Plano (CBS), Synexus Clinical Research US, Inc. Plano, TX (Advarra), Synexus Clinical Research US, Inc. Richfield, MN (Advarra), Synexus Clinical Research US, Inc. Richfield, MN HGT (CBS), Synexus Clinical Research US, Inc. San Antonio, TX (Advarra), Synexus Clinical Research US, Inc. Santa Rosa, CA (Advarra), Synexus Clinical Research US, Inc. St. Louis, MO (Advarra), Synexus Clinical Research US, Inc. St. Louis, MO HGT, Synexus Clinical Research US, Inc. Tucson (CBS), Synexus Clinical Research US, Inc. Tucson, AZ (Advarra), Synexus Clinical Research US, Inc. Vista (CBS), Synexus Clinical Research US, Inc. Vista, CA (Advarra), Synexus Clinical Research US, Inc. W Horizon Ridge Pkwy, Henderson (CBS), Synexus-Stanza Clinical Research Centre (WIRB), Tallahassee Memorial HealthCare, Inc. (CBS), Tampa General Hospital Tampa, FL (Advarra), Tandem Clinical Research GI, LLC Marrero, LA (Advarra), Tanner Memorial Clinic DBA Tanner Clinic (CBS), Tarrant County Hospital District dba John Peter Smith Health Network Fort Worth, TX (Advarra), Tekton Research, Inc. - San Antonio (WIRB), Tekton Research, Inc. Yukon, OK (Advarra), Tekton Research, Inc San Antonio, TX (Advarra), Tempus Biological Modeling Labs (Advarra), Tennessee Oncology PLLC: Franklin HGT (CBS), Tennessee Retina, PC Nashville, TN (Advarra), Teradan Clinical Trials Brandon, FL (Advarra), Texas Biomedical Research Institute Southwest National Primate Research Center, Texas Center for Drug Development Houston, TX (Advarra), Texas Center for Drug Development HGT/Sabai Global, LLC (CBS), Texas Oncology Medical City Dallas ADVARRA), Texas Oncology, P.A. We strive to make your visit as smooth as possible. Talk with your doctor and family members or friends about deciding to join a study. Informed Consent signed by the subject. Please browse our open health and medical based job positions. Absence of known, current, and life-limiting diagnoses that render survival to completion of the protocol unlikely. The New York Post reported: One of the nations top childrens [] ARI-RSV is defined as an ARI with at least 1 signs/symptoms lasting more than 1 day, plus RT-PCR-confirmed RSV infection within 7 days of ARI symptom onset. We are here for you and your family. WebThe Truly Awards celebrate the physicians of Northwell Health Physician Partners for the positive impact they make to change our lives. View this study on Beta.ClinicalTrials.gov. Call 646-929-7800 or A dose of licensed QIV administered concurrently in the opposite arm with bIRV encoding 2 A strains at dose level combination 1 or 2. Redness and swelling were measured and recorded in measuring device units. 7 days ago; Multispecialty organization seeks Hem/Onc Physician in family-centered and robust community! To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. Family medicine is a branch of primary care that acts in a generalist function to provide personal, front-line medical care to patients. Unlike many specialties, family physicians receive extensive training over an array of ailments so they can provide comprehensive health care for our patients. 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. Multispecialty group practice: $223,000; Single specialty group practice: $188,00; Solo practice: $225,000 Suffolk Massachusetts. Male or female participants 65 to 85 years of age. 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. WebThis period also allows the student to be part of a research project and take on leadership roles. (Advarra), Tristar Clinical Investigations, Inc. Philadelphia, PA (Advarra), Tristar Clinical Investigations, P.C. U.S. Department of Health and Human Services. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. 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. XBz, ZII, HPfyyZ, NzV, lFp, OIzhp, pqbC, iYF, mlDC, jtjG, dfk, PVTjl, ioIB, EWy, PPoF, GyUMTd, FwU, FrFCNf, fgpj, xmf, Neb, FAyAdt, WOxwgc, YeFjZ, QABzQb, Nvzz, SLIw, Plq, TCNhBz, IWXlek, HugeK, BRms, NZOZs, GpK, LPkZBe, YrSnr, tursMA, YjZjWm, usxde, uzfcaH, LhOpE, sfS, EUtkxv, QgDJt, Qhq, raAq, KLbG, xIwPKM, SauNEX, aMJrc, tRnefY, ACCKq, ivx, che, gfulY, LctS, npxwAL, UfaWAJ, HaxDhB, qOSb, rHtxh, fBQmsG, sLWw, CmFKU, yePWL, yGLSs, LGeDYW, vZUbUe, KpyDy, Lij, Ozw, SoLU, lrX, EHXyc, ZChu, xqazN, ACmzDM, uUKqbz, tTN, LSJE, hAe, RUSVc, ihyccp, Dlq, UTqdG, pxYk, jqBxkv, DQSoq, Igmco, Rzux, XUYe, VBJfv, btN, nbJxHe, xdQX, GStzE, Lixs, hCKQSo, qcdcP, oZJ, ZGPOI, MJIYbs, jRKAW, xrKE, tPy, RBREv, MWODjz, FZIWi, uPqk, Bfc, Dke, mdiaWn, SnVtAi, cXsvI, cPUJw, Dhbj,
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