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Clinical Trials (131)
| Trial | Conditions | Phase | Status | Enrollment | Design | Drug |
|---|---|---|---|---|---|---|
| NCT05600777 A 24-Week Study of the Efficacy and Safety of BLU-5937 in Adults With Refractory Chronic Cough | Cough, Refractory Chronic Cough | P3 | Active | 975 | RCT, Double-blind | BLU-5937, Placebo |
| NCT05599191 A 52-Week Study of the Efficacy and Safety of BLU-5937 in Adults With Refractory Chronic Cough | Cough, Refractory Chronic Cough | P3 | Active | 825 | RCT, Double-blind | BLU-5937, Placebo |
| NCT06065462 Safety and Efficacy of Targeting PP2A in Ovarian Clear Cell Carcinoma Using Dostarlimab and LB-100 | Ovarian Clear Cell Carcinoma | P1P2 | Recruiting | 21 | Open-label | Dostarlimab, LB-100 |
| NCT03833479 TSR-042 as Maintenance Therapy for Patients With High-risk Locally Advanced Cervical Cancer After Chemo-radiation | Cervical Cancer, Advanced Cancer | P2 | Active | 134 | RCT, Open-label | TSR-042 |
| NCT05489237 First-in-human Study of IDRX-42 in Participants With Metastatic and/or Unresectable Gastrointestinal Stromal Tumors | Gastrointestinal Neoplasms, Gastrointestinal Stromal Tumor (GIST) | P1 | Active | 276 | Open-label | IDRX-42 |
| NCT00160394 Comparison of Duac® Gel And Differin® Gel in Mild to Moderate Acne Vulgaris | Acne Vulgaris | P4 | Completed | 130 | RCT, Single-blind | Duac® Gel / Differin® Gel |
| NCT00887484 A Comparative Study of the Tolerability of Two Combination Therapies for the Treatment of Acne | Acne Vulgaris | P4 | Completed | 50 | RCT, Single-blind | BENZOYL PEROXIDE/ CLINDAMYCIN, BENZOYL PEROXIDE/ ADAPALENE |
| NCT00964366 Study to Determine and Compare the Tolerance and Irritation Potential of Topical Acne Medications | Acne Vulgaris | P4 | Completed | 53 | RCT, Single-blind | clindamycin and benzoyl peroxide, Dapsone gel |
| NCT01015638 Compare the Tolerance of Clindamycin 1% /Benzoyl Peroxide (BPO) 5% Gel to Clindamycin 1.2%/ BPO 2.5% Topical Medications | Acne Vulgaris | P4 | Completed | 36 | RCT, Single-blind | Clindamycin and BPO 5% gel, Clindamycin phosphate and benzoyl peroxide 2.5% gel. |
| NCT00837213 Comparative Efficacy and Safety of Benzoyl Peroxide Used in Combination With Clindamycin vs. Benzoyl Peroxide Used in Combination With Clindamycin and Doxycycline in the Treatment of Moderate Acne | Acne | P4 | Completed | 33 | RCT, Single-blind | Benzoyl peroxide with clindamycin, Benzoyl peroxide with clindamycin and doxycycline |
| NCT01933698 Bioequivalence of Two Commercial Amoxicillin Suspensions | Bioequivalence of Amoxicillin | P4 | Completed | 25 | RCT, Double-blind | amoxicillin |
| NCT01597492 A Study to Evaluate the Effect of Belimumab on Vaccine Responses in Subjects With Systemic Lupus Erythematosus (SLE) | Systemic Lupus Erythematosus | P4 | Completed | 79 | RCT, Open-label | Belimumab plus Early Vaccination, Belimumab plus Late Vaccination |
| NCT00841776 Comparative Antimicrobial Efficacy of Two Topical Acne Therapies for the Treatment of Facial Acne | Acne | P4 | Completed | 54 | RCT, Single-blind | Duac, Ziana gel |
| NCT00842153 Evaluation of the Efficacy and Tolerability of Clobetasol Propionate Foam Compared to Vehicle Foam | Psoriasis | P4 | Completed | 58 | RCT, Double-blind | Clobetasol propionate foam, Vehicle foam |
| NCT00693654 Comparative Study of the Efficacy of SARNA Sensitive Lotion for Treatment of Uremic Itch in Adult Hemodialysis Patients | Pruritis | P4 | Completed | 28 | RCT, Double-blind | Sarna, Cetaphil |
| NCT01706250 U0289-401: Eight Week, Split-face, Study to Determine and Compare the Efficacy and Tolerability of MAXCLARITY™ II to PROACTIV™ | Acne Vulgaris | P4 | Completed | 20 | RCT, Single-blind | — |
| NCT01632241 Efficacy and Safety of Belimumab in Black Race Patients With Systemic Lupus Erythematosus (SLE) | Systemic Lupus Erythematosus | P4 | Completed | 503 | RCT, Double-blind | Placebo plus standard therapy, Belimumab 10 mg/kg plus standard therapy, Standard therapy |
| NCT02524665 8 Week Study to Evaluate and Compare the Efficacy and Tolerability of MAXCLARITY II and MURAD To Treat Acne | Acne Vulgaris | P4 | Completed | 20 | RCT, Single-blind | — |
| NCT00926367 Two-week Study to Compare the Tolerance and Irritation Potential of Two Combination Topical Gel Acne Medications | Acne Vulgaris | P4 | Completed | 52 | RCT, Single-blind | Clindamycin and benzoyl peroxide, benzoyl peroxide 2.5% and adapalene 0.1% gel |
| NCT00702507 Prospective Two-Year Study to Assess Miconazole Nitrate Resistance in Neonates and Infants | Diaper Rash | P4 | Completed | 200 | Open-label | 0.25 % Miconazole Nitrate Ointment |
| NCT00757523 Evaluation of the Effectiveness, Safety, and Tolerability of Duac Akne Gel and Epiduo Gel in the Treatment of Facial Acne Vulgaris | Acne Vulgaris | P4 | Completed | 382 | RCT, Single-blind | Epiduo Gel, Duac Gel |
| NCT00852761 A Study to Evaluate the Efficacy and Tolerability of Topical Therapies for the Condition of Plaque-Type Psoriasis | Plaque-Type Psoriasis | P4 | Completed | 34 | RCT, Single-blind | Olux-E Foam, Clobex lotion |
| NCT01706263 U0289-402: An Open Label, 8 Week Study to Evaluate the Efficacy and Tolerability of MAXCLARITY II in Subjects With Acne | Acne Vulgaris | P4 | Completed | 28 | Open-label | MAXCLARITY II (2.5% BPO) Foam Cleanser, MAXCLARITY II (2.5% BPO) Foam Treatment, MAXCLARITY II (0.5% Salicylic Acid) Toner Foam |
| NCT01745133 Olux E Foam and Sorilux Foam Combination Therapy for the Maintenance of Treatment Response in Patients With Moderate Plaque Psoriasis | Psoriasis | P4 | Completed | 63 | RCT, Single-blind | vehicle foam, calcipotriene, calcipotriene + clobetasol propionate |
| NCT01323673 Ethanol-Free Clobetasol Propionate Foam 0.05% (Olux-E Foam) vs Vehicle Foam in the Treatment of Chronic Hand Dermatitis. | Dermatitis, Chronic | P4 | Completed | 125 | RCT, Double-blind | clobetasol propionate 0.05%, Vehicle / Placebo |
| NCT00240513 Study Comparing Acne in Patients Taking Oral Minocycline to Patients Taking Minocycline Plus Topical Tretinoin | Acne Vulgaris | P4 | Terminated | 38 | RCT, Single-blind | Minocycline, Minocycline plus tretinoin |
| NCT01016977 A Phase 4, Single-Blind, Randomized, Study to Compare the Tolerability and Efficacy of 0.1% Tazorac Cream When Used in Combination With Either Duac Gel or Acanya Gel for the Treatment of Facial Acne Vulgaris | Acne Vulgaris | P4 | Completed | 40 | RCT, Single-blind | Clindamycin 1%/Benzoyl Peroxide 5% and 0.1% tazarotene, clindamycin phosphate 1.2%/benzoyl peroxide 2.5% and 0.1% tazarotene |
| NCT00964223 A Study to Evaluate Tolerability of Two Topical Drug Products in the Treatment of Facial Acne | Acne Vulgaris | P4 | Completed | 28 | RCT, Single-blind | Clindamycin and benzoyl peroxide gel (Duac® Topical Gel), benzoyl peroxide and adapalene gel (EPIDUO™ Gel) |
| NCT00703846 STUDY TO ASSESS THE LONG-TERM SAFETY OF EXTINA (KETOCONAZOLE) FOAM, 2% | Dermatitis, Seborrheic | P4 | Completed | 498 | Open-label | Ketoconazole |
| NCT00807014 Evaluation of Quality of Life, Efficacy, and Tolerance of Duac® Gel Compared to Differin® Gel in the Treatment of Acne | Acne Vulgaris | P4 | Completed | 169 | RCT, Single-blind | Duac Gel, Differin gel |
| NCT00832364 Trial of an Injectable Biologic and U0279 as Combination Therapy for Severe Plaque-Type Psoriasis | Plaque Psoriasis | P4 | Withdrawn | — | RCT, Single-blind | Acitretin (also called U0279), Placebo, Etanercept |
| NCT01228409 Low-Dose (17.5 mg/Day) Acitretin: Comparable Efficacy Without the Side Effects? | Psoriasis | P4 | Unknown | 20 | Open-label | Acitretin 17.5 mg/day |
| NCT00828464 Study to Evaluate Safety, Efficacy and Tolerability of Clobetasol Propionate for Chronic Hand Dermatitis | Hand Dermatosis | P4 | Completed | 30 | Open-label | clobetasol propionate |
| NCT01639339 Efficacy and Safety of Belimumab in Patients With Active Lupus Nephritis | Lupus Nephritis | P3 | Completed | 448 | RCT, Double-blind | Placebo plus standard therapy, Belimumab 10 mg/kg plus standard therapy, Standard therapy |
| NCT00712933 A Continuation Trial for Subjects With Lupus That Completed Protocol HGS1006-C1056 or HGS1006-C1057 | Systemic Lupus Erythematosus | P3 | Completed | 738 | Open-label | belimumab |
| NCT02014584 Sexual Function in Men Receiving Dutasteride for Androgenetic Alopecia | Alopecia | P3 | Completed | 117 | RCT, Double-blind | Dutasteride, Placebo |
| NCT00776919 Trial of Clindamycin / Benzoyl Peroxide Gel in Subjects With Acne | Acne Vulgaris | P3 | Completed | 1,315 | RCT, Double-blind | clindamycin / benzoyl peroxide gel, clindamycin gel, BPO gel, vehicle gel |
| NCT01663623 Belimumab in Remission of VASculitis | Vasculitis | P3 | Completed | 106 | RCT, Double-blind | Placebo, Belimumab 10 mg/kg, Azathioprine |
| NCT00088673 Evaluation of 3APS in Patients With Mild to Moderate Alzheimer's Disease | Alzheimer Disease | P3 | Unknown | 950 | RCT, Double-blind | 3APS |
| NCT01017120 A Study to Evaluate the Safety and Efficacy of Tazarotene Foam, 0.1%, in Subjects With Common Facial Acne | Acne Vulgaris | P3 | Completed | 742 | RCT, Double-blind | Tazarotene Foam, Vehicle Foam |
| NCT00282724 Efficacy and Safety of Two Doses of Liarozole vs. Placebo for the Treatment of Lamellar Ichthyosis | Ichthyosis, Lamellar | P2P3 | Completed | 98 | RCT, Double-blind | Liarozole |
| NCT01484496 A Study of Belimumab Administered Subcutaneously in Subjects With Systemic Lupus Erythematosus (SLE) | Systemic Lupus Erythematosus | P3 | Completed | 839 | RCT, Double-blind | Placebo, Belimumab 200 mg SC, Standard therapy |
| NCT00356915 Itraconazole Tablets Vs. Itraconazole Capsules vs. Placebo in Onychomycosis of the Toenail. | Onychomycosis | P3 | Completed | 1,381 | RCT, Single-blind | Itraconazole 100mg capsules, Itraconazole 200mg tablets, Placebo tablets |
| NCT00817063 Efficacy and Safety of a Retinoid in the Treatment of Severe Chronic Hand Eczema | Eczema | P3 | Completed | 599 | RCT, Double-blind | alitretinoin, Placebo |
| NCT00689481 Study to Compare U0267 Against Vehicle in Subjects With Plaque-type Psoriasis Two of Two Phase 3 Studies | Psoriasis | P3 | Completed | 323 | RCT, Double-blind | U0267 Foam, Vehicle foam |
| NCT00724867 A Continuation Trial for Subjects With Lupus Who Completed Protocol HGS1006-C1056 in the United States | Systemic Lupus Erythematosus | P3 | Completed | 268 | Open-label | Belimumab 1 mg/kg, Belimumab 10 mg/kg |
| NCT00689117 A Clinical Study to Evaluate the Safety and Effectiveness of an Investigational Product Called CT Gel | Acne Vulgaris, Acne | P3 | Completed | 1,649 | RCT, Double-blind | CT Gel, Clindamycin Gel (clindamycin ), Tretinoin Gel (tretinoin), Vehicle Gel |
| NCT02101268 Efficacy of Momelotinib Versus Best Available Therapy in Anemic or Thrombocytopenic Subjects With Primary Myelofibrosis (MF), Post-polycythemia Vera MF, or Post-essential Thrombocythemia MF | Primary Myelofibrosis (PMF), Post-polycythemia Vera (Post-PV) | P3 | Completed | 156 | RCT, Open-label | Momelotinib, Best Available Therapy (BAT) |
| NCT01017146 A Study to Evaluate the Safety and Efficacy of Tazarotene Foam, 0.1%, in Subjects With Common Facial Acne - W0260-301 | Acne Vulgaris | P3 | Completed | 744 | RCT, Double-blind | Tazarotene foam, Vehicle Foam |
| NCT00891982 A Clinical Study to Evaluate the Tolerability of a Topical Antibiotic and Retinoid Used in a Combined Regimen With a BPO Wash | Acne Vulgaris | P3 | Completed | 60 | RCT, Single-blind | CTGel/ BPO Wash, Soap Free Cleanser and CTGel |
| NCT00314912 Open-Label Extension of the Phase III Study With Tramiprosate (3APS) in Patients With Mild to Moderate Alzheimer's Disease | Alzheimer's Disease | P3 | Unknown | 650 | Open-label | Tramiprosate (3APS) |
| NCT00852540 Retapamulin Versus Linezolid in the Treatment of SITL and Impetigo Due to MRSA | Skin Infections, Bacterial | P3 | Completed | 410 | RCT, Double-blind | Retpamulin Ointment, 1%, Linezolid |
| NCT00217763 European Study of 3APS in Mild to Moderate Alzheimer's Disease Patients | Alzheimer's Disease | P3 | Unknown | 930 | RCT, Double-blind | 3APS |
| NCT00688519 Study to Compare U0267 Against Vehicle in Subjects With Plaque-type Psoriasis One of Two Phase 3 Studies | Psoriasis | P3 | Completed | 336 | RCT, Double-blind | U0267, Vehicle |
| NCT00035334 Study of the Safety and Efficacy of NC-503 in Secondary (AA) Amyloidosis | Secondary (AA) Amyloidosis, Rheumatoid Arthritis | P2P3 | Completed | 150 | RCT, Double-blind | NC-503 (Anti-amyloidotic (AA) Agent) |
| NCT01969838 Momelotinib Versus Ruxolitinib in Subjects With Myelofibrosis | Primary Myelofibrosis, Post-Polycythemia Vera Myelofibrosis | P3 | Completed | 432 | RCT, Double-blind | Momelotinib, Ruxolitinib, Placebo to match momelotinib, Placebo to match ruxolitinib |
| NCT04173494 A Study of Momelotinib Versus Danazol in Symptomatic and Anemic Myelofibrosis Participants (MOMENTUM) | Primary Myelofibrosis, Post-polycythemia Vera Myelofibrosis | P3 | Completed | 195 | RCT, Double-blind | Momelotinib, Placebo to match danazol, Danazol, Placebo to match momelotinib |
| NCT01139580 The Purpose of This Study is to Demonstrate the Safety and Effectiveness of Calcipotriene Foam in Subjects With Scalp and Body Psoriasis | Psoriasis | P3 | Completed | 363 | RCT, Double-blind | Calcipotriene Foam, Vehicle Foam |
| NCT02101021 Gemcitabine and Nab-paclitaxel Combined With Momelotinib in Participants With Previously Untreated Metastatic Pancreatic Ductal Adenocarcinoma | Metastatic Pancreatic Ductal Adenocarcinoma | P3 | Terminated | 25 | Double-blind | Momelotinib, Placebo to match momelotinib, Nab-paclitaxel, Gemcitabine |
| NCT02515630 Momelotinib in Transfusion-Dependent Adults With Primary Myelofibrosis (PMF) or Post-polycythemia Vera or Post-essential Thrombocythemia Myelofibrosis (Post-PV/ET MF) | Primary Myelofibrosis (PMF), Post-polycythemia Vera (Post-PV) Myelofibrosis | P2 | Completed | 41 | Open-label | MMB |
| NCT02378038 PNT2258 for Treatment of Patients With Richter's Transformation (Brighton) | Richter's Transformation | P2 | Terminated | 5 | Open-label | PNT2258 |
| NCT01258608 Study of Mapatumumab in Combination With Sorafenib in Subjects With Advanced Hepatocellular Carcinoma | Carcinoma, Hepatocellular | P1P2 | Completed | 101 | RCT, Double-blind | Mapatumumab, Placebo, Sorafenib |
| NCT01998828 Safety and Efficacy of Momelotinib in Subjects With Polycythemia Vera or Essential Thrombocythemia | Polycythemia Vera, Essential Thrombocythemia | P2 | Terminated | 39 | RCT, Open-label | Momelotinib |
| NCT01236638 Extension Study Evaluating the Long Term Safety and Efficacy Study of CYT387 in Primary Myelofibrosis (PMF) or Post-polycythemia Vera (PV) or Post-essential Thrombocythemia (ET) | Primary Myelofibrosis, Post-Polycythemia Vera Myelofibrosis | P2 | Completed | 120 | Open-label | Momelotinib |
| NCT00920556 A Clinical Study to Assess the Safety and Activity of SRT501 Alone or in Combination With Bortezomib in Patients With Multiple Myeloma | Multiple Myeloma | P2 | Terminated | 24 | Open-label | 5.0g SRT501, Bortezomib |
| NCT00937326 Clinical Study to Assess the Safety and Pharmacokinetics of SRT2104 in Type 2 Diabetic Human Subjects | Diabetes Mellitus, Type 2 | P2 | Completed | 227 | RCT, Double-blind | SRT2104, Placebo |
| NCT00725439 An Open Label Trial to Assess the Safety and Efficacy of Oral R115866 in the Treatment Facial Acne | Acne | P2 | Completed | 16 | Open-label | Talarozole |
| NCT01733238 Study of PNT2258 for Treatment of Relapsed or Refractory Non-Hodgkin's Lymphoma | Lymphoma, Non-Hodgkin's | P2 | Completed | 13 | Open-label | PNT2258 |
| NCT00675857 A Phase IIa Proof-of-concept Study of NC-503 in Patients With Type II Diabetes | Diabetes Mellitus, Type 2, Metabolic Syndrome X | P2 | Completed | 200 | RCT, Double-blind | NC-503 (eprodisate disodium) |
| NCT00725348 An Open-Label, Multi-Center Trial in the Treatment of Subjects With Moderate to Severe Plaque Type Psoriasis | Psoriasis | P2 | Completed | 19 | Open-label | Talarozole |
| NCT03979638 A Dose Escalation Study of BLU-5937 in Unexplained or Refractory Chronic Cough | Chronic Refractory Cough | P2 | Terminated | 68 | RCT, Double-blind | BLU-5937, Placebo |
| NCT00716144 Dose Ranging Study of the Safety and Efficacy of R115966 in Plaque Psoriasis | Psoriasis | P2 | Completed | 176 | RCT, Double-blind | Talarozole |
| NCT04693195 A Multiple-Dose Study of BLU-5937 in Chronic Pruritus Associated With Atopic Dermatitis | Chronic Pruritus, Atopic Dermatitis | P2 | Completed | 142 | RCT, Double-blind | BLU-5937, Placebo |
| NCT00056238 Cerebril™ in Patients With Lobar Hemorrhage Related to Cerebral Amyloid Angiopathy | Stroke, Neurologic Diseases, General | P2 | Completed | 30 | RCT, Double-blind | NC-758 (Anti amyloidotic [Aß] agent) |
| NCT02226965 PNT2258 for Treatment of Patients With r/r DLBCL (Wolverine) | Lymphoma, Diffuse Large B-Cell | P2 | Completed | 45 | Open-label | PNT2258 |
| NCT00713609 Safety and Efficacy Study of Clindamycin/Benzoyl Peroxide/Tazarotene Cream in Subjects With Acne | Acne Vulgaris | P2 | Completed | 591 | RCT, Double-blind | Benzoyl peroxide gel, Clindamycin gel, Tazarotene cream, Vehicle gel, Vehicle cream |
| NCT02797964 A Phase 1/2 Trial of SRA737 in Subjects With Advanced Cancer | Advanced Solid Tumors or Non-Hodgkin's Lymphoma (NHL) | P1P2 | Completed | 107 | Open-label | SRA737 |
| NCT02797977 A Phase 1/2 Trial SRA737 in Combination With Gemcitabine and Cisplatin or Gemcitabine Alone in Advanced Cancer Subjects | Advanced Solid Tumors | P1P2 | Completed | 153 | Open-label | SRA737, gemcitabine, cisplatin, SRA737, gemcitabine |
| NCT01649765 Pediatric Lupus Trial of Belimumab Plus Background Standard Therapy | Systemic Lupus Erythematosus | P2 | Completed | 93 | RCT, Double-blind | Belimumab 10 mg/kg |
| NCT01154101 Study of the Clinical Activity, Safety, and Tolerability of SRT2104 in Subjects With Moderate to Severe Plaque-Type Psoriasis | Psoriasis | P2 | Completed | 40 | RCT, Double-blind | Placebo, SRT2104 |
| NCT00730405 Efficacy and Safety Study of 4 Dose Regimens of Oral Albaconazole in Subjects With Distal Subungual Onychomycosis | Onychomycosis | P2 | Completed | 582 | RCT, Double-blind | Albaconazole 100mg, Albaconazole 200mg, Albaconazole 400mg, Albaconazole 400mg, Placebo 400 mg |
| NCT01245140 Efficacy of Alitretinoin Treatment in Patients With Pustular Form of Psoriasis | Psoriasis | P2 | Completed | 33 | RCT, Double-blind | alitretinoin, Placebo |
| NCT00583362 A Continuation Trial for Subjects With Systemic Lupus Erythematosus That Have Completed Protocol LBSL02 | Systemic Lupus Erythematosus | P2 | Completed | 298 | Open-label | Belimumab |
| NCT01423058 Safety Study Evaluating Twice-Daily Administration of Momelotinib in Primary Myelofibrosis or Post-Polycythemia Vera or Post-Essential Thrombocythemia Myelofibrosis | Primary Myelofibrosis, Post-Polycythemia Vera | P1P2 | Completed | 61 | Open-label | Momelotinib |
| NCT02124746 Long-term Safety and Efficacy of Momelotinib in Subjects With Primary Myelofibrosis, Post-polycythemia Vera Myelofibrosis, Post-essential Thrombocythemia Myelofibrosis, Polycythemia Vera or Essential Thrombocythemia | Primary Myelofibrosis, Post-Polycythemia Vera Myelofibrosis | P2 | Completed | 87 | Open-label | Momelotinib |
| NCT00935987 Safety and Efficacy Study of CYT387 in Primary Myelofibrosis (PMF) or Post-polycythemia Vera (PV) or Post-essential Thrombocythemia (ET) | Primary Myelofibrosis, Post-Polycythemia Vera Myelofibrosis | P1P2 | Completed | 166 | Open-label | CYT387 |
| NCT02673619 A Study to Evaluate Clinical Effect, Pharmacokinetics , Safety, and Tolerability of Umeclidinium in Palmar Hyperhidrosis Subjects | Hyperhidrosis | P2 | Completed | 58 | RCT, Double-blind | Umeclidinium, Vehicle |
| NCT04678206 Evaluation of the Efficacy and Safety of BLU-5937 in Adults With Refractory Chronic Cough | Refractory Chronic Cough | P2 | Completed | 310 | RCT, Double-blind | BLU-5937, Placebo |
| NCT01604863 A Study of HGS1036 in Combination With Chemotherapy in Subjects With Advanced Solid Malignancies | Cancer | P1 | SUSPENDED | 54 | Open-label | HGS1036 + Paclitaxel + Carboplatin, HGS1036 + Cisplatin + Etoposide, HGS1036 + Docetaxel |
| NCT01112787 A Study to Evaluate the Irritation Potential of Tazarotene Foam on Skin in Healthy Volunteers | Acne Vulgaris | P1 | Completed | 39 | RCT, Double-blind | Tazarotene Foam, Vehicle Foam, Sodium Laural Sulfate, Distilled Water |
| NCT05959447 Evaluation of the Potential Drug-drug Interactions Between Gemfibrozil or Dabigatran Etexilate and Camlipixant | Cough, Healthy | P1 | Completed | 45 | Open-label | Camlipixant, Dabigatran etexilate, Gemfibrozil |
| NCT01340911 A Study in Healthy Male Volunteers to Investigate Different Doses of a New Drug for the Treatment of Metabolic Diseases | Diabetes Mellitus, Type 2 | P1 | Completed | 78 | RCT, Single-blind | SRT3025, Placebo |
| NCT02017899 A Phase 1, Dose Escalation Study, to Evaluate a New Shigella Sonnei Vaccine in Healthy Adults. | Shigellosis | P1 | Completed | 50 | RCT, Double-blind | S. sonnei 1790GAHB, Placebo |
| NCT00920803 A Clinical Study to Assess the Safety, Pharmacokinetics, and Pharmacodynamics of SRT501 in Subjects With Colorectal Cancer and Hepatic Metastases | Neoplasms, Colorectal | P1 | Completed | 9 | RCT, Double-blind | Placebo, SRT501 |
| NCT05899829 Evaluation of the Effect of Rifampin and Rabeprazole on the Pharmacokinetics of Camlipixant | Cough, Healthy | P1 | Completed | 42 | Open-label | Camlipixant, Rabeprazole, Rifampin |
| NCT01416376 Effect of Multiple Dose Levels of SRT2379 on Endotoxin-Induced Inflammation | Sepsis | P1 | Completed | 39 | RCT, Double-blind | SRT2379, Placebo |
| NCT06179537 Evaluation of the Pharmacokinetics and Safety of BLU-5937 in Healthy Adult Japanese and Caucasian Subjects | Healthy | P1 | Completed | 34 | RCT, Double-blind | BLU-5937 |
| NCT02206763 Erlotinib and Momelotinib for the Treatment of Epidermal Growth Factor Receptor (EGFR) Mutated EGFR Tyrosine Kinase Inhibitor (TKI) Naive Metastatic Non-Small Cell Lung Cancer (NSCLC) | EGFR Mutated EGFR TKI Naive Metastatic NSCLC | P1 | Terminated | 11 | Open-label | Momelotinib (MMB), Erlotinib |
| NCT01132443 W0261-101: A Phase 1, Single Center, Randomized, Open-Label Study to Evaluate the Bioavailability of Clindamycin From Clindamycin 1%-Benzoyl Peroxide 3% Gel, Topical Gel (Clindamycin 1%- Benzoyl Peroxide 5%), and Once Daily Gel (Clindamycin 1%-Benzoyl Peroxide 5%) in Subjects With Acne | Acne Vulgaris | P1 | Completed | 72 | RCT, Open-label | Clindamycin 1%-Benzoyl Peroxide (BPO) 3% Gel, |
| NCT00938275 A Clinical Study to Assess the Effect of Food and Gender on the Pharmacokinetics of SRT2104 Administered as an Oral Suspension or Capsule Formulation to Normal Healthy Volunteers | Diabetes Mellitus, Type 2 | P1 | Completed | 20 | RCT, Open-label | 0.5g SRT2104 |
| NCT00712855 A Study of Mapatumumab in Combination With Sorafenib in Subjects With Advanced Hepatocellular Carcinoma | Hepatocellular Carcinoma | P1 | Completed | 23 | Open-label | mapatumumab, sorafenib |
| NCT01031108 A Clinical Trial to Assess the Safety of Oral SRT2104 and Its Effects on Vascular Dysfunction in Otherwise Healthy Cigarette Smokers and Subjects With Type 2 Diabetes Mellitus | Diabetes Mellitus, Type 2 | P1 | Completed | 38 | RCT, Double-blind | Placebo, SRT2104 |
| NCT00933530 A Clinical Study to Assess the Safety and Pharmacokinetics of SRT2104 in Normal Healthy Male Volunteers | Diabetes Mellitus, Type 2, Healthy Volunteer | P1 | Completed | 43 | RCT, Single-blind | SRT2104, Placebo |
| NCT05244759 Mass Balance Recovery, Absorption, Metabolism and Excretion of [14C]-BLU-5937 | Healthy | P1 | Completed | 6 | Open-label | [14C]-BLU-5937 |
| NCT03638180 BLU-5937: First-in-Human, Single and Multiple Doses Escalation, Safety, Tolerability, Pharmacokinetics and Food Effect | Cough | P1 | Completed | 90 | RCT, Double-blind | BLU-5937, Placebo |
| NCT01115322 A Study to Evaluate the Potential of Tazarotene Foam to Cause a Reaction When Applied to the Skin and Exposed to Light on Healthy Volunteers | Acne Vulgaris | P1 | Completed | 38 | RCT, Single-blind | Tazarotene Foam without irradiation, Tazarotene Foam with UVA and UVB irradiation, Tazarotene Foam with UVA, UVB, and visible light, Vehicle Foam without irradiation, Vehicle Foam with UVA and UVB irradiation, Vehicle Foam with UVA and UVB and visible light irradiation, No Treatment without irradiation, No Treatment with UVA and UVB irradiation, No Treatment with UVA and UVB and visible light irradiation |
| NCT02411162 A Single Dose Phase I Exploratory Study in Healthy Volunteers With GSK2894512 Cream | Dermatitis, Atopic | P1 | Completed | 15 | Open-label | Combination therapy GSK2894512 Cream A + GSK2894512 Cream B, Combination therapy Vehicle Cream A + Vehicle Cream B |
| NCT00509275 A Study to Evaluate Efficacy and Safety of Three W0027 Regimens in the Treatment of Moccasin Type Tinea Pedis (MTTP) | Tinea Pedis | P1 | Completed | 120 | RCT, Double-blind | W0027, Placebo |
| NCT01262911 Effect of SRT2379 on Endotoxin-Induced Inflammation | Sepsis | P1 | Completed | 17 | RCT, Double-blind | SRT2379, Placebo |
| NCT02034500 Evaluate a New Shigella Sonnei Vaccine Administered Either by Intradermal, Intranasal or Intramuscular Route in Healthy Adults | Shigellosis | P1 | Completed | 52 | RCT, Double-blind | S. sonnei 1790GAHB, Placebo |
| NCT01039883 A Study to Compare the Blood Levels of Albaconazole in Healthy Subjects Who Have Received a Single Dose of 400 mg Albaconazole as a Tablet Versus Albaconazole as a Capsule | Onychomycosis | P1 | Completed | 40 | RCT, Open-label | Albaconazole tablet 400mg, Albaconazole 100mg capsules, then albaconazole 400mg tablet |
| NCT06222892 A Study of Camlipixant in Male and Female Healthy Participants and Participants With Hepatic Impairment Aged 18-75 Years of Age | Cough | P1 | Completed | 32 | Open-label | Camlipixant |
| NCT01453491 A Phase 1b Study to Assess the Safety and Anti-inflammatory Effects of Two Different Doses of SRT2104 in Patients With Ulcerative Colitis | Colitis, Ulcerative | P1 | Completed | 17 | RCT, Double-blind | SRT2104 |
| NCT02244489 Momelotinib Combined With Capecitabine and Oxaliplatin in Adults With Relapsed/Refractory Metastatic Pancreatic Ductal Adenocarcinoma | Relapsed/Refractory Metastatic Pancreatic Ductal Adenocarcinoma | P1 | Terminated | 16 | Open-label | Momelotinib (MMB), Capecitabine, Oxaliplatin |
| NCT00695071 Study to Assess Blood Levels of Itraconazole During a Two-Week Period | Healthy | P1 | Completed | 16 | Open-label | Itraconazole |
| NCT06497517 A Study to Investigate the Effect of Food on Camlipixant Concentrations in Healthy Participants | Cough | P1 | Completed | 14 | RCT, Open-label | GSK5464714- Camlipixant |
| NCT02258607 Efficacy and Safety of Momelotinib Combined With Trametinib in Adults With Metastatic KRAS-mutated Non-Small Cell Lung Cancer (NSCLC) Who Have Failed Platinum-Based Chemotherapy Preceded by a Dose-finding Lead-in Phase | Relapsed Metastatic KRAS-Mutated Non-Small Cell Lung Cancer | P1 | Terminated | 21 | Open-label | Momelotinib (MMB), Trametinib |
| NCT01114841 A Study To Evaluate The Contact Sensitization Potential Of Tazarotene Foam On Skin In Healthy Volunteers | Acne Vulgaris | P1 | Completed | 254 | RCT, Single-blind | Tazarotene Foam, Vehicle Foam |
| NCT05570539 Assessment of the Pharmacokinetics of BLU-5937 Extended Release Prototypes and a BLU-5937 Immediate Release Reference Formulation | Cough, Healthy | P1 | Completed | 30 | Open-label | BLU-5937 IR, BLU-5937 ER |
| NCT01191775 A Study of PNT2258 in Patients With Advanced Solid Tumors | Cancer, Lymphoma | P1 | Completed | 22 | Open-label | PNT2258 |
| NCT01984775 A Study to Evaluate the Irritation Potential of GSK2894512 Cream on Skin in Healthy Subjects | Psoriasis | P1 | Completed | 52 | RCT, Double-blind | GSK2894512 cream, Vehicle cream, Positive control, Negative control |
| NCT01929278 W0265-103: A Single-Center, Evaluator-Blinded, Randomized, Placebo Controlled, Phase 1 Clinical Trial Evaluating The Phototoxic Potential Of Topically Applied Clindamycin 1.0% - Tretinoin 0.025% Gel (Ct Gel) In Healthy Volunteers | Acne Vulgaris | P1 | Completed | 37 | RCT, Single-blind | CT Gel (clindamycin 1% and tretinoin 0.025%) |
| NCT01702493 A Study to Assess the Relative Bioavailability of New Oral Formulations of SRT2104 in Healthy Male Volunteers | Psoriasis | P1 | Completed | 16 | RCT, Open-label | Cap SRT2104, Tab SRT2104 slow release, Tab SRT2104 intermediate release, Tab SRT2104 fast release, Selected formulations of SRT2104 from Part 1, Selected formulations of SRT2104 from Part 1 single alternative dose |
| NCT01014962 A Study of the Effects of Increasing Doses of a Drug for the Treatment of Nail Fungus | Onychomycosis | P1 | Completed | 24 | RCT, Double-blind | Albaconozole, Placebo, Albaconozole, Placebo, Albaconozole, Placebo |
| NCT00937872 A Clinical Study to Evaluate the Pharmacokinetics and the Absolute Bioavailability of SRT2104 Given as a 250mg Oral Suspension and Intravenous Microdose of 100 µg Carbon-14 Radio-labeled SRT2104 in Healthy Male Subjects | Diabetes Mellitus, Type 2 | P1 | Completed | 9 | Open-label | 250 mg SRT2104 Suspension, Carbon-14 radio-labeled SRT2104 |
| NCT01019603 A Study to Evaluate the Bioavailability of Tazarotene Foam, 0.1%, and Tazorac Gel, 0.1%, in Subjects With Acne Vulgaris | Acne Vulgaris | P1 | Completed | 30 | RCT, Open-label | Tazarotene, Tazaroc Gel |
| NCT00719121 Study on Anti-inflammatory Effects of Topical R115866 Gel | Cutaneous Inflammation | P1 | Completed | 12 | RCT, Single-blind | Talarozole, Differin™, 0.1% adapalene gel |
| NCT01119651 A Study to Evaluate the Potential of Tazarotene Foam to Cause an Allergic Reaction When Applied to the Skin and Exposed to Light on Healthy Volunteers. | Acne Vulgaris | P1 | Completed | 59 | RCT, Single-blind | Tazarotene (Patch application in Challenge Phase) |
| NCT00931086 Expanded Access Trial of Belimumab Antibody in RA Patients Who Were Previously Treated Under HGS Protocol LBRA99 | Rheumatoid Arthritis | NO_LONGER_AVAILABLE | — | — | belimumab | |
| NCT01446237 U0289-405: An Open-Label, 12-Week Study to Evaluate the Efficacy and Safety of the Acne System (Benzoyl Peroxide 2.5%, Salicylic Acid 0.5%) in Subjects With Acne | Acne Vulgaris | N/A | Completed | 125 | Open-label | — |
| NCT01858792 A Pooled Analysis of the HGS1006-C1056 (BLISS-52) and HGS1006-C1057 (BLISS-76) Studies | Lupus Erythematosus, Discoid | Completed | 1 | — | Belimumab 1 mg/kg, Belimumab 10 mg/kg |