순번 | 임상시험 제목 | 적응증 | 연구설계 | 의뢰자/실시기관 | 임상단계 | NCT No | 개시일자 |
---|---|---|---|---|---|---|---|
1 | A Study to Evaluate Adverse Events and Change in Disease Activity in Participants Between 18 to 75 Years of Age Treated With Intravenous (IV) Infusion and Subcutaneous (SC) Injections of ABBV-154 for Moderately to Severely Active Crohn's Disease | Crohn's Disease | Drug: ABBV-154|Drug: Placebo | AbbVie | Phase 2 | NCT05068284 | 2022-01-31 |
2 | A Study of MK-1084 as Monotherapy and in Combination With Pembrolizumab (MK-3475) in Participants With KRASG12C Mutant Advanced Solid Tumors (MK-1084-001) | Advanced Solid Tumors | Drug: MK-1084|Biological: Pembrolizumab | Merck Sharp & Dohme LLC | Phase 1 | NCT05067283 | 2021-12-17 |
3 | Pembrolizumab/Placebo Plus Paclitaxel With or Without Bevacizumab for Platinum-resistant Recurrent Ovarian Cancer (MK-3475-B96/KEYNOTE-B96/ENGOT-ov65) | Ovarian Cancer|Carcinoma, Ovarian Epithelial|Fallopian Tube Neoplasms | Biological: Pembrolizumab|Drug: Paclitaxel|Drug: Bevacizumab|Other: Placebo for pembrolizumab|Drug: Docetaxel | Merck Sharp & Dohme LLC | Phase 3 | NCT05116189 | 2021-12-13 |
4 | NTLA-2002 in Adults With Hereditary Angioedema (HAE) | Hereditary Angioedema | Biological: Biological NTLA-2002|Other: Normal Saline IV Administration | Intellia Therapeutics | Phase 1|Phase 2 | NCT05120830 | 2021-12-10 |
5 | A Study of JNJ-73763989, JNJ-64300535, and Nucleos(t)Ide Analogs in Virologically Suppressed, Hepatitis B e Antigen (HBeAg)- Negative Participants With Chronic Hepatitis B Virus Infection | Hepatitis B, Chronic | Drug: JNJ-73763989|Biological: JNJ-64300535|Drug: ETV monohydrate|Drug: Tenofovir disoproxil|Drug: TAF | Janssen Research & Development, LLC | Phase 1 | NCT05123599 | 2021-12-06 |
6 | A Study to Evaluate HB0034 in Healthy Adult Participants | Healthy | Drug: HB0034|Drug: Placebo | Shanghai Huaota Biopharmaceutical Co., Ltd. | Phase 1 | NCT05064345 | 2021-12-03 |
7 | MK-1654 in Infants and Children at Increased Risk for Severe Respiratory Syncytial Virus (RSV) Disease (MK-1654-007) | RSV Infection | Biological: MK-1654|Biological: Palivizumab|Biological: Placebo | Merck Sharp & Dohme LLC | Phase 3 | NCT04938830 | 2021-11-30 |
8 | Immunogenicity and Safety Study of SK SARS-CoV-2 Recombinant Nanoparticle Vaccine (GBP510) Adjuvanted With AS03 (COVID-19) | Covid19 | Biological: GBP510 adjuvanted with AS03 (Receptor-Binding Domain(RBD) 25ug/dose)|Biological: ChAdOx1-S not less than 2.5 횞 10^8 infectious units | SK Bioscience Co., Ltd.|International Vaccine Institute|GlaxoSmithKline|Coalition for Epidemic Preparedness Innovations | Phase 3 | NCT05007951 | 2021-08-30 |
9 | Safety and Immunogenicity of VLA2001 Adults Aged ??6 Years | SARS-CoV-2 Virus Infection | Biological: VLA2001 | Valneva Austria GmbH | Phase 3 | NCT04956224 | 2021-08-09 |
10 | A Study of an Adenovirus Serotype 26 Pre-fusion Conformation-stabilized F Protein (Ad26. RSV. preF) Based Respiratory Syncytial Virus (RSV) Vaccine in the Prevention of Lower Respiratory Tract Disease in Adults Aged 60 Years and Older | Respiratory Syncytial Viruses|Lower Respiratory Tract Disease | Biological: Adenovirus serotype 26 (Ad26)-based respiratory syncytial virus (RSV). preF|Biological: Placebo | Janssen Vaccines & Prevention B.V. | Phase 3 | NCT04908683 | 2021-07-21 |