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AbbVie Inc randomisation schedule
Randomisation Schedule, supplied by AbbVie Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/randomisation+schedule/randomisation+schedule/10__1002_slash_14651858__cd014805__pub2-1574-1-13
Average 90 stars, based on 1 article reviews
randomisation schedule - by Bioz Stars, 2026-09
90/100 stars

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Related Articles

Generated:

Article Title: Interventions for fatigue in inflammatory bowel disease
Article Snippet: The patient number and group of each stratum were assigned by a central randomisation schedule generated by AbbVie (Chicago, IL, USA) using WebRando software for randomisation and ClinPhone, an interactive voice and web response system for patient allocation. .. The subject randomisation schedule was generated by a designated person in the AbbVie statistics department who was not involved in the rest of the study". .. Allocation concealment (selection bias) Low risk "All patients were randomised centrally using an interactive voice and web response system (ClinPhone)".

Article Title: Upadacitinib for the treatment of active non-radiographic axial spondyloarthritis (SELECT-AXIS 2): a randomised, double-blind, placebo-controlled, phase 3 trial
Article Snippet: .. Interactive response technology was used to assign patients a unique identification number at the screening visit based on a randomisation schedule generated by the sponsor’s (AbbVie; North Chicago, IL, USA) statistics department. ..

Article Title: Safety and efficacy of upadacitinib in patients with rheumatoid arthritis and inadequate response to conventional synthetic disease-modifying anti-rheumatic drugs (SELECT-NEXT): a randomised, double-blind, placebo-controlled phase 3 trial
Article Snippet: Methods This study is a double-blind, placebo-controlled trial at 150 sites in 35 countries.. We enrolled patients aged 18 years or older with active rheumatoid arthritis for 3 months or longer, who had received csDMARDs for at least 3 months with a stable dose for at least 4 weeks before study entry, and had an inadequate response to at least one of the following csDMARDs: methotrexate, sulfasalazine, or leflunomide.. Using interactive response technology, we randomly assigned patients receiving stable background csDMARDs (2:2:1:1) to receive a once-daily extendedrelease formulation of upadacitinib 15 mg or 30 mg, or placebo, for 12 weeks.

Sequencing:

Article Title: Systemic pharmacological treatments for chronic plaque psoriasis: a network meta‐analysis
Article Snippet: .. Random sequence generation (selection bias) , Low risk , Quote (p 2 & Appendix): "The randomisation schedule was prepared by the Statistics Department of AbbVie, US. Randomization was performed using an adequate block size.“ Comment: probably done. .. Allocation concealment (selection bias) , Low risk , Quote (p 2 & Appendix): “An interactive voice/web response system determined patient randomisation. The randomisation schedule was prepared by the Statistics Department of AbbVie, US. Randomization was performed using an adequate block size.“ Comment: probably done.

Article Title: Systemic pharmacological treatments for chronic plaque psoriasis: a network meta‐analysis
Article Snippet: .. Risk of bias Bias Authors' judgement Support for judgement Random sequence generation (selection bias) Low risk Quote (p 2 & Appendix): "The randomisation schedule was prepared by the Statistics Department of AbbVie, US. ..

Selection:

Article Title: Systemic pharmacological treatments for chronic plaque psoriasis: a network meta‐analysis
Article Snippet: .. Random sequence generation (selection bias) , Low risk , Quote (p 2 & Appendix): "The randomisation schedule was prepared by the Statistics Department of AbbVie, US. Randomization was performed using an adequate block size.“ Comment: probably done. .. Allocation concealment (selection bias) , Low risk , Quote (p 2 & Appendix): “An interactive voice/web response system determined patient randomisation. The randomisation schedule was prepared by the Statistics Department of AbbVie, US. Randomization was performed using an adequate block size.“ Comment: probably done.

Article Title: Systemic pharmacological treatments for chronic plaque psoriasis: a network meta‐analysis
Article Snippet: .. Risk of bias Bias Authors' judgement Support for judgement Random sequence generation (selection bias) Low risk Quote (p 2 & Appendix): "The randomisation schedule was prepared by the Statistics Department of AbbVie, US. ..

Article Title: Systemic pharmacological treatments for chronic plaque psoriasis: a network meta‐analysis
Article Snippet: Random sequence generation (selection bias) , Low risk , Quote (p 2 & Appendix): "The randomisation schedule was prepared by the Statistics Department of AbbVie, US. Randomization was performed using an adequate block size.“ Comment: probably done. .. Allocation concealment (selection bias) , Low risk , Quote (p 2 & Appendix): “An interactive voice/web response system determined patient randomisation. The randomisation schedule was prepared by the Statistics Department of AbbVie, US. Randomization was performed using an adequate block size.“ Comment: probably done. .. Blinding of participants and personnel (performance bias) All outcomes , Low risk , Quote (p 2 & Appendix): “Patients in Period A were randomised 4:1 to receive adalimumab 40 mg every‐other‐week (following a single 80 mg dose), or matching placebo...All AbbVie personnel with direct oversight of the conduct and management of the trial (with the exception of the drug supply team), the investigator, study‐site personnel and the patient remained blinded to each patient’s treatment throughout the 12 week blinded period of the study." Comment: probably done.

Blocking Assay:

Article Title: Systemic pharmacological treatments for chronic plaque psoriasis: a network meta‐analysis
Article Snippet: .. Random sequence generation (selection bias) , Low risk , Quote (p 2 & Appendix): "The randomisation schedule was prepared by the Statistics Department of AbbVie, US. Randomization was performed using an adequate block size.“ Comment: probably done. .. Allocation concealment (selection bias) , Low risk , Quote (p 2 & Appendix): “An interactive voice/web response system determined patient randomisation. The randomisation schedule was prepared by the Statistics Department of AbbVie, US. Randomization was performed using an adequate block size.“ Comment: probably done.

Article Title: Systemic pharmacological treatments for chronic plaque psoriasis: a network meta‐analysis
Article Snippet: Random sequence generation (selection bias) , Low risk , Quote (p 2 & Appendix): "The randomisation schedule was prepared by the Statistics Department of AbbVie, US. Randomization was performed using an adequate block size.“ Comment: probably done. .. Allocation concealment (selection bias) , Low risk , Quote (p 2 & Appendix): “An interactive voice/web response system determined patient randomisation. The randomisation schedule was prepared by the Statistics Department of AbbVie, US. Randomization was performed using an adequate block size.“ Comment: probably done. .. Blinding of participants and personnel (performance bias) All outcomes , Low risk , Quote (p 2 & Appendix): “Patients in Period A were randomised 4:1 to receive adalimumab 40 mg every‐other‐week (following a single 80 mg dose), or matching placebo...All AbbVie personnel with direct oversight of the conduct and management of the trial (with the exception of the drug supply team), the investigator, study‐site personnel and the patient remained blinded to each patient’s treatment throughout the 12 week blinded period of the study." Comment: probably done.



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Image Search Results


CONSORT 2025 checklist of information to include when reporting a randomised trial

Journal: The BMJ

Article Title: CONSORT 2025 explanation and elaboration: updated guideline for reporting randomised trials

doi: 10.1136/bmj-2024-081124

Figure Lengend Snippet: CONSORT 2025 checklist of information to include when reporting a randomised trial

Article Snippet: The allocation sequence number is recorded by the research team on the data collection form (DCF), the database and in the participant’s medical record.” “LabCorp Drug Development (a subcontractor to the IWRS [interactive web response system] vendor) generated the live randomisation schedules.

Techniques: Sequencing, Generated, Blocking Assay

Items to include when reporting a randomised trial in a journal abstract

Journal: The BMJ

Article Title: CONSORT 2025 explanation and elaboration: updated guideline for reporting randomised trials

doi: 10.1136/bmj-2024-081124

Figure Lengend Snippet: Items to include when reporting a randomised trial in a journal abstract

Article Snippet: The allocation sequence number is recorded by the research team on the data collection form (DCF), the database and in the participant’s medical record.” “LabCorp Drug Development (a subcontractor to the IWRS [interactive web response system] vendor) generated the live randomisation schedules.

Techniques: Generated

Five core elements of a defined outcome with examples

Journal: The BMJ

Article Title: CONSORT 2025 explanation and elaboration: updated guideline for reporting randomised trials

doi: 10.1136/bmj-2024-081124

Figure Lengend Snippet: Five core elements of a defined outcome with examples

Article Snippet: The allocation sequence number is recorded by the research team on the data collection form (DCF), the database and in the participant’s medical record.” “LabCorp Drug Development (a subcontractor to the IWRS [interactive web response system] vendor) generated the live randomisation schedules.

Techniques:

Steps in a typical  randomisation  process

Journal: The BMJ

Article Title: CONSORT 2025 explanation and elaboration: updated guideline for reporting randomised trials

doi: 10.1136/bmj-2024-081124

Figure Lengend Snippet: Steps in a typical randomisation process

Article Snippet: The allocation sequence number is recorded by the research team on the data collection form (DCF), the database and in the participant’s medical record.” “LabCorp Drug Development (a subcontractor to the IWRS [interactive web response system] vendor) generated the live randomisation schedules.

Techniques: Sequencing

Information required to document the flow of participants through each stage of a randomised trial for the primary outcome

Journal: The BMJ

Article Title: CONSORT 2025 explanation and elaboration: updated guideline for reporting randomised trials

doi: 10.1136/bmj-2024-081124

Figure Lengend Snippet: Information required to document the flow of participants through each stage of a randomised trial for the primary outcome

Article Snippet: The allocation sequence number is recorded by the research team on the data collection form (DCF), the database and in the participant’s medical record.” “LabCorp Drug Development (a subcontractor to the IWRS [interactive web response system] vendor) generated the live randomisation schedules.

Techniques:

Example of good reporting: Treatments after  randomisation  in patients in an intention-to-treat population

Journal: The BMJ

Article Title: CONSORT 2025 explanation and elaboration: updated guideline for reporting randomised trials

doi: 10.1136/bmj-2024-081124

Figure Lengend Snippet: Example of good reporting: Treatments after randomisation in patients in an intention-to-treat population

Article Snippet: The allocation sequence number is recorded by the research team on the data collection form (DCF), the database and in the participant’s medical record.” “LabCorp Drug Development (a subcontractor to the IWRS [interactive web response system] vendor) generated the live randomisation schedules.

Techniques: