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Midatech begins dosing in first human trial of cancer drug Q-Octreotide
Midatech has commenced initial dosing in the first in-human study of its sustained release product Q-Octreotide (MTD201) for the treatment of carcinoid cancer and acromegaly.
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Janssen's Erleada shown to reduce PSA progression by 94% in nmCRPC patients
By PBR Staff Writer
Janssen Pharmaceutical's androgen receptor inhibitor Erleada (apalutamide) succeeded in a phase 3 trial by significantly cutting down the risk of prostate specific antigen (PSA) progression in patients having non-metastatic castration-resistant prostate cancer (nmCRPC).
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Pfizer’s Lyrica meets primary endpoint in phase 3 pediatric epilepsy trial
Pfizer has reported positive top-line results from a phase 3 study, which assessed the use of Lyrica (pregabalin) oral solution CV as adjunctive therapy for partial onset seizures in pediatric epilepsy patients one month to less than four years of age.
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IDMC recommends to expand Tiziana’s phase 2a trial of Milciclib
Tiziana Life Sciences announces that the independent data monitor committee (IDMC) completed a second, interim analysis of tolerability data from the first eleven treated patients and recommended expansion of the initial cohort to continue enrolment of an additional 20 patients to complete the trial.
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AstraZeneca’s COPD drug Fasenra fails to meet primary endpoint in phase III trial
By PBR Staff Writer
AstraZeneca’s respiratory drug Fasenra (benralizumab) has failed to meet its primary endpoint in the Galathea phase III trial.
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Merck to invest $125m in Moderna Therapeutics
By PBR Staff Writer
Merck has agreed to invest $125m in Moderna Therapeutics under a new agreement that expands the firms’ 2016 partnership to develop messenger RNA (mRNA) cancer vaccines.
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Merck signs deal with SFJ on colorectal cancer drug development
Merck has entered into a development agreement with US-based SFJ Pharmaceuticals Group (SFJ) to develop abituzumab in metastatic colorectal cancer.
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Karyopharm’s multiple myeloma drug Selinexor succeeds in phase 2b study
By PBR Staff Writer
Karyopharm Therapeutics’ selinexor, an oral selective inhibitor of nuclear export (SINE) compound, has succeeded in a phase 2b study by showing a 25.4% overall response rate (ORR) in heavily pretreated patients with refractory multiple myeloma.
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Allergan’s ubrogepant migraine drug succeeds in second phase 3 trial
By PBR Staff Writer
Allergan’s migraine drug ubrogepant has succeeded in a phase 3 trial by meeting its co-primary endpoints for a 50mg dose.
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Vertex launches phase 3 trials of VX-445/Tezacaftor/Ivacaftor combo in cystic fibrosis
Vertex Pharmaceuticals has initiated two phase 3 studies of VX-445, tezacaftor and ivacaftor as an investigational triple combination regimen for people with cystic fibrosis (CF).
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ADC Therapeutics terminates ADCT-502 program targeting HER2 expressing solid tumors
ADC Therapeutics (ADCT) has terminated the phase I clinical trial to assess its antibody drug conjugate (ADC) ADCT-502 in patients with advanced solid tumors with HER2 expression.
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AstraZeneca’s lung cancer combo fails in phase III trial
AstraZeneca’s lung cancer combo of Imfinzi (durvalumab) plus tremelimumab has failed to deliver desired results in a phase III trial, called ARCTIC, in patients with locally-advanced or metastatic non-small cell lung cancer (NSCLC) who had more than two prior treatments.
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Prothena scraps development of AL amyloidosis drug
By PBR Staff Writer
Prothena is stopping the development of AL amyloidosis treatment NEOD001 following unfavorable results in the phase 2b Pronto study.
Contract Research & Services > Clinical Trials > News
Helperby Therapeutics’ combination antibiotic therapy is effective against WHO critical priority pathogen in phase 1 study
Helperby Therapeutics has announced Phase I results on the tolerability, pharmacokinetics, pharmacodynamics and efficacy of AZT and colistin both alone and as a combined therapy, against multi-drug resistant Enterobacteriaceae (CRE), one of the most serious drug resistant pathogens.
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Boehringer Ingelheim, Lilly, University of Oxford to study empagliflozin in chronic kidney disease
Boehringer Ingelheim and Eli Lilly and Company have entered into an academic collaboration with the University of Oxford to assess the effects of Jardiance (empagliflozin) on heart and kidney disease in adults with chronic kidney disease.
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