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Jasper C Ho, Ader Q Asaria, Elizabeth Munroe

Vasopressors are a mainstay of treatment for patients with shock.1 Historically, prolonged or high-dose vasopressors have been administered through central venous catheters (CVCs), a practice that stems from safety concerns following early reports of severe ischemic tissue injury due to peripheral vasopressor extravasation.2–4 Peripheral intravenous (PIV) access in these reports was often via metal cannulae secured with the venous […]

Robin Deterding, ERS 2022: Findings from the InPedILD Trial

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Published Online: Sep 30th 2022

The InPedILD trial was a phase 3, double-blind placebo-controlled trial investigating nintedanib in children and adolescents with fibrosing interstitial lung diseases (ClinicalTrials.gov: NCT04093024). We were delighted to speak to Dr. Robin Deterding (University of Colorado; Children’s Hospital Colorado, Aurora, CO, USA) to discuss the aims, design, eligibility criteria and findings from the phase 3 study.

The abstract ‘Nintedanib in children and adolescents with fibrosing interstitial lung disease: the InPedILD trial.‘ was presented at ERS 2022, 4–6 September, 2022.

Questions

  1. What were the aims, design and eligibility criteria of the InPedILD trial? (0:35)
  2. What were the primary and secondary efficacy and safety endpoints, and how well were they achieved? (2:41)
  3. On the basis of these findings, what further studies are planned? (7:43)

Disclosures: Robin Deterding discloses consulting for Boehringer Ingelheim; receiving grant/ research support from Boehringer Ingelheim; and serving on advisory boards for Boehringer Ingelheim.

Support: Interview and filming supported by Touch Medical Media Ltd. Interview conducted by Victoria Jones.

Filmed in coverage of the ERS meeting 2022.

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