Study of DCR-PHXC-101 in Normal Healthy Volunteers and Patients With Primary Hyperoxaluria
A Placebo-Controlled, Single-Blind, Single-Center Phase 1 Study in Normal Healthy Volunteers and Open-Label Multi-Center Study in Patients With Primary Hyperoxaluria to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single Ascending Doses of DCR-PHXC Solution for Injection (Subcutaneous Use)
Sponsor: Dicerna Pharmaceuticals, Inc., a Novo Nordisk company
A PHASE1 clinical study on Primary Hyperoxaluria, this trial is completed. The trial is conducted by Dicerna Pharmaceuticals, Inc., a Novo Nordisk company and has accumulated 13 data snapshots since 2017. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.
Status Flow
Change History
13 versions recorded-
Oct 2024 — Present [monthly]
Completed PHASE1
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Sep 2024 — Oct 2024 [monthly]
Completed PHASE1
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Aug 2024 — Sep 2024 [monthly]
Completed PHASE1
-
Jul 2024 — Aug 2024 [monthly]
Completed PHASE1
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May 2023 — Jul 2024 [monthly]
Completed PHASE1
▶ Show 8 earlier versions
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Jan 2021 — May 2023 [monthly]
Completed PHASE1
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Feb 2020 — Jan 2021 [monthly]
Completed PHASE1
Status: Active Not Recruiting → Completed
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Aug 2019 — Feb 2020 [monthly]
Active Not Recruiting PHASE1
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Mar 2019 — Aug 2019 [monthly]
Active Not Recruiting PHASE1
Status: Recruiting → Active Not Recruiting
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Nov 2018 — Mar 2019 [monthly]
Recruiting PHASE1
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Oct 2018 — Nov 2018 [monthly]
Recruiting PHASE1
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Jun 2018 — Oct 2018 [monthly]
Recruiting PHASE1
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Jan 2018 — Jun 2018 [monthly]
Recruiting PHASE1
First recorded
Dec 2017
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Dicerna Pharmaceuticals, Inc., a Novo Nordisk company
For direct contact, visit the study record on ClinicalTrials.gov .