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Study ID Status Title Patient Level Data
205335 Completed A phase IV, open-label, single-center study to evaluate long term immunogenicity up to 10 years after the first booster immunization with Tick Borne Encephalitis vaccine in adults who received 1 of 3 different primary vaccination schedules
205336 Active not recruiting A Phase IV, Open-Label, Multi-Center Study to Evaluate the Safety and the 1-year Persistence of Antibody Response Among Children Who Received 4 Doses of the GSK MenACWY Conjugate Vaccine at 2, 4, 6 and 12 Months of Age in South Korea
205341 Recruiting A Multicenter Post Marketing Surveillance Study to monitor the safety of Novartis Meningococcal ACWY conjugate vaccine(MenACWY-CRM) administered according to the prescribing information to healthy subjects from 2 months to 55 years of age in the Republic of South Korea.
205352 Recruiting A Phase 3b, Controlled, Open-Label, Multi-Center Study to Evaluate Safety and Immunogenicity of a Single Dose of GlaxoSmithKline’s Meningococcal ACWY Conjugate Vaccine (Menveo), Administered to Healthy Individuals 15 through 55 years of age, approximately 4-6 years after primary ACWY vaccination
205369 Active not recruiting Impact of rotavirus vaccination on hospital pressures at a large paediatric hospital in the UK: an ecological study
205421 Completed A Phase 2, Non-Randomized, Controlled, Open-Label, Parallel-Group, Extension Study to Evaluate the Immunogenicity and Safety of the Second Dose of GBS Trivalent Vaccine in Healthy Non-pregnant Subjects.
205431 Withdrawn Determination of SPF, before and after immersion in water, for a cosmetic product at minimum of 3 subjects.
205432 Withdrawn Determination of SPF, before and after immersion in water, for a cosmetic product at minimum of 3 subjects
205433 Not yet recruiting Determination of SPF, before and after immersion in water, for a cosmetic product at minimum of 3 subjects.
205434 Not yet recruiting A comparative, open-label, randomized, and controlled clinical efficacy trial for preview evaluation of the skin oiliness control for three cosmetics products
205496 Active not recruiting A Phase 1, Randomized, Observer-Blind, Dosage-Escalation Study to Evaluate the Safety and Immunogenicity of an Aluminium Hydroxide/LHD153R Adjuvanted Meningococcal C-CRM197 Conjugate Vaccine Compared to Aluminium Hydroxide Adjuvanted Meningococcal C-CRM197 Conjugate Vaccine in Healthy Adults (18-45 years of age).
205523 Completed Feasibility study for identifying a sero-correlate of protection against invasive Group B Streptococcus disease in newborns and young infants aged less than 90 days.
205531 Recruiting Menveo® pregnancy registry: an observational study on the safety of Menveo exposure in pregnant women and their offspring
205533 Recruiting 4CMenB pregnancy registry: an observational study of the safety of 4CMenB exposure in pregnant women and their offspring.
205534 Active not recruiting Post-licensure observational safety surveillance study of quadrivalent meningococcal ACWY conjugate vaccine MenACWY-CRM (Menveo®) in children 2 months through 23 months of age.
205540 Recruiting A randomised, double-blind, placebo-controlled, parallel group, 8-week treatment study to investigate the safety, pharmacodynamics, and effect of the TLR7 agonist, GSK2245035, on the allergen-induced asthmatic response in subjects with mild allergic asthma
205613 Recruiting A Phase 2b Open-Label Multi-Center Study Assessing the Immunological Persistence of Antibodies at Approximately 2 years After the last Meningococcal Vaccination in Study V102_15 (NCT02212457) and the Response to a Booster dose of GSK MenABCWY or Meningococcal Serogroup B Vaccines, in Healthy Adolescents
205633 Not yet recruiting Severe Asthma: Characterizing Patient Impacts of Frequent/Chronic Use of Oral Corticosteroids
205634 Completed A phase IV, open label, single-center extension study, to evaluate the long-term persistence of immune responses after post-exposure prophylaxis with purified chicken-embryo cell rabies Vaccine in Chinese children
205636 Completed A Randomized, Parallel-Group, Placebo-Controlled Study to Evaluate the Local Nasal Tolerability and Safety of 1146A in Healthy Adult Subjects
205637 Withdrawn An open-label, multicenter, randomized, parallel group, single-dose study to assess the short term efficacy and safety of paracetamol 500 mg + phenylephrine HCl 10 mg + pheniramine maleate 20 mg + vitamin C 200 mg powder for oral solution in subjects with symptoms of an upper respiratory tract infection.
205638 Withdrawn An open-label, multicenter, randomized, parallel group, single-dose study to assess the short term efficacy and safety of paracetamol 500 mg + phenylephrine HCl 10 mg + vitamin C 200 mg powder for oral solution in subjects with symptoms of an upper respiratory tract infection
205639 Recruiting Meta-analysis of the risk of autoimmune thyroiditis diseases, Guillain-Barré Syndrome, and Inflammatory Bowel Disease with Cervarix Vaccination
205643 Completed PGx7654: Pharmacogenetic investigation of the association of the beta2-adrenergic receptor (ADRB2) Thr164Ile variant with risk of hospitalization due to asthma exacerbations
205654 Not yet recruiting MALARONE Pediatric Combination Tablets Special Drug Use Investigation

 

 

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