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Correction: Methodology of the SORENTO clinical trial: a prospective, randomised, active-controlled phase 3 trial assessing the efficacy and safety of high exposure octreotide subcutaneous depot (CAM2029) in patients with GEP-NET
Trials volume 25, Article number: 297 (2024)
Correction: Trials 25, 58 (2024)
https://doi.org/10.1186/s13063-023-07834-8
Following publication of the original article [1], we have been notified that a correction is needed on page 3, paragraph 2 as shown below:
Incorrect statement: “Additionally, CAM2029 administration can be undertaken by the patient or carer themselves using a pre-filled pen, whereas administration of both octreotide LAR and lanreotide ATG requires medical assistance.”
Correct statement: “Additionally, CAM2029 administration can be undertaken by the patient or carer themselves using a pre-filled pen, whereas administration of octreotide LAR requires medical assistance. For patients who receive a stable dose of lanreotide ATG, the product can be administered either by the patient or by a trained person (Reference Somatuline Autogel 60 mg, solution for injection in a prefilled syringe—Summary of Product Characteristics (SmPC)—(emc) (medicines.org.uk)).”
The original article has been corrected.
Reference
Singh S, et al. Methodology of the SORENTO clinical trial: a prospective, randomised, active-controlled phase 3 trial assessing the efficacy and safety of high exposure octreotide subcutaneous depot (CAM2029) in patients with GEP-NET. Trials. 2024;25:58. https://doi.org/10.1186/s13063-023-07834-8.
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Singh, S., Ferone, D., Capdevila, J. et al. Correction: Methodology of the SORENTO clinical trial: a prospective, randomised, active-controlled phase 3 trial assessing the efficacy and safety of high exposure octreotide subcutaneous depot (CAM2029) in patients with GEP-NET. Trials 25, 297 (2024). https://doi.org/10.1186/s13063-024-08146-1
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DOI: https://doi.org/10.1186/s13063-024-08146-1