Injection Site Pain Comparison of Excipient Solutions
NCT04482725 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 108
Last updated 2021-10-19
Summary
The purpose of this study is to investigate different solutions used to inject drugs under the skin. The solutions used in the study do not contain the drugs they will be used for, but they do contain excipients, which are inactive substances added to drug solutions to ensure the stability (shelf life and correct activity) of the drug product. The excipients are considered 'inactive substances' compared to the drug, but they may cause an undesirable effect at the injection site in the form of pain. However, their pain-causing potential has never been tested in a systematic way. The purpose of the study is to determine if there is a difference in the injection site pain experience after an injection under the skin (subcutaneous) with 12 different study products. These study products are excipient solutions, which are substances in medications next to the active substance. None of the 12 products include active medication. This study will be performed in 108 healthy male and female volunteers.
Conditions
Interventions
- OTHER
-
Trial product 1
Buffering agent: N/A Isotonic agent: NaCl 9.0 mg/mL
- OTHER
-
Trial product 2
Buffering agent: Disodium hydrogen phosphate, dihydrate 1.42 mg/mL Isotonic agent: NaCl 8.25 mg/mL
- OTHER
-
Trial product 3
Buffering agent: Disodium hydrogen phosphate dihydrate 1.42 mg/mL Isotonic agent: Propylene glycol 18.5 mg/mL
- OTHER
-
Trial product 4
Buffering agent: Disodium hydrogen phosphate dihydrate 1.42 mg/mL Isotonic agent: Glycerol 22.0 mg/mL
- OTHER
-
Trial product 5
Buffering agent: Disodium hydrogen phosphate dihydrate 1.42 mg/mL Isotonic agent: Mannitol 44.0 mg/mL
- OTHER
-
Trial product 6
Buffering agent: Disodium hydrogen phosphate dihydrate 1.42 mg/mL Isotonic agent: Sucrose 82.0 mg/mL
- OTHER
-
Trial product 7
Buffering agent: Disodium hydrogen phosphate dihydrate 1.42 mg/mL Isotonic agent: a,a-Trehalose, dihydrate 90.0 mg/mL
- OTHER
-
Trial product 8
Buffering agent: Disodium hydrogen phosphate dihydrate 5.34 mg/mL Isotonic agent: NaCl 6.72 mg/mL
- OTHER
-
Trial product 9
Buffering agent: Tris 2.4 mg/mL Isotonic agent: Propylene glycol 19 mg/mL
- OTHER
-
Trial product 10
Buffering agent: Glutamic acid 0.74 mg/mL Isotonic agent: Glycerol 24.0 mg/mL
- OTHER
-
Trial product 10
Buffering agent: Sodium Acetate, trihydrate 0.68 mg/mL Isotonic agent: Glycerol 24.0 mg/mL
- OTHER
-
Trial product 12
Buffering agent: Glutamic acid 0.46 mg/mL, Disodium hydrogen phosphate, dihydrate 2.00 mg/mL Isotonic agent: Glycerol 15 mg/mL, NaCl 2.5 mg/mL
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Clinical Reporting Anchor and Disclosur (1452) · Novo Nordisk A/S
Study Design
- Allocation
- RANDOMIZED
- Purpose
- OTHER
- Masking
- QUADRUPLE
- Model
- SEQUENTIAL
Eligibility
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2020-07-20
- Primary Completion
- 2020-09-24
- Completion
- 2020-09-25
Countries
- Netherlands
Study Locations
More Related Trials
-
A Multiple Dose Study Investigating Pharmacokinetics and Pharmacodynamics of Subcutaneous NNC0363-0845 in Participants With Type 1 Diabetes Pharmacokinetics and Pharmacodynamics: How Insulin NNC0363-0845 is Transported Throughout the Body and How It Works
NCT05134987 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Test How Insulin NNC0471-0119 H Works in the Body in Participants With Type 2 Diabetes When Given by an Insulin Pump
NCT07068295 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Test How Insulin NNC0471-0119 H Works in the Body in Participants With Type 1 Diabetes When Given by an Insulin Pump
NCT06809621 ·Status: COMPLETED ·Phase: PHASE1
-
Patient Experiences With Injection Needles
NCT02531776 ·Status: COMPLETED ·Phase: NA
-
Feasibility Study of the Effect of Intra-Dermal Insulin Injection on Blood Glucose Levels After Eating
NCT00553488 ·Status: COMPLETED ·Phase: PHASE2
-
Localisation of Potential Insulin Deposits in Normal Weight and Obese Diabetics Using 6 mm and 12 mm Long Needles
NCT00871416 ·Status: COMPLETED ·Phase: PHASE3
-
Feasibility Study for Training Pump Naïve Subjects To Use The Paradigm® System And Evaluate Effectiveness
NCT00530023 ·Status: COMPLETED ·Phase: PHASE4
-
Multi-day (3) In-patient Evaluation of Intradermal Versus Subcutaneous Basal and Bolus Insulin Infusion
NCT01557907 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Investigating the Pharmacokinetics and Pharmacodynamics of Recombinant Human Insulin Administered by Dry Powder Inhaler
NCT00426920 ·Status: UNKNOWN ·Phase: PHASE1
-
Pharmacokinetic and Early Efficacy of OPT101 in Patients With Type 1 Diabetes Mellitus
NCT06964087 ·Status: RECRUITING ·Phase: PHASE2
-
Safety Study to Assess Whether Proinsulin Peptide Injections Can Slow or Stop the Body Damaging Its Own Insulin-making Cells in the Pancreas in Patients Newly Diagnosed With Type 1 Diabetes
NCT01536431 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Efficacy and Safety of Continuous Subcutaneous Insulin Infusion of Faster-acting Insulin Aspart Compared to NovoRapid® in Adults With Type 1 Diabetes
NCT02825251 ·Status: COMPLETED ·Phase: PHASE3
-
Pharmacology of Insulin Injected With Jet-Injection
NCT00983775 ·Status: COMPLETED ·Phase: NA
-
A Study of LY900027 Given by Insulin Pump to Participants With Type 1 Diabetes Mellitus
NCT04161976 ·Status: COMPLETED ·Phase: PHASE1
-
Evaluating the Use of Two Different Needles in Subjects With Diabetes
NCT00569426 ·Status: COMPLETED ·Phase: PHASE4
-
Subcutaneous Pharmacokinetic Evaluation of Monomeric Insulin and Lyumjev in Adults With Type 1 Diabetes
NCT07090824 ·Status: RECRUITING ·Phase: PHASE1
-
A Research Study of a New Medicine NNC0363-1063 in Healthy Participants and Participants With Type 1 Diabetes
NCT06685185 ·Status: COMPLETED ·Phase: PHASE1
-
Comparing Intensive and Standard Training for Human Insulin Inhalation Powder (HIIP)
NCT00099515 ·Status: COMPLETED ·Phase: PHASE2
-
Study Comparing Effectiveness of Intraperitoneal Insulin Administration to Subcutaneous Insulin Administration
NCT00211536 ·Status: COMPLETED ·Phase: PHASE3
-
A Trial Investigating the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Subcutaneous NNC0143-0406 A 0.6 mmol/L in Subjects With Type 1 Diabetes
NCT02612844 ·Status: COMPLETED ·Phase: PHASE1
-
Pharmacokinetics/Dynamics of Basal (Continuous) Insulin Infusion Administered Either Intradermally or Subcutaneously
NCT01061216 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Insulin by Jet-injection for Hyperglycemia in Diabetes
NCT01947556 ·Status: COMPLETED ·Phase: NA
-
A Research Study of a New Medicine NNC0363-1063 in Participants With Type 1 Diabetes
NCT07305805 ·Status: RECRUITING ·Phase: PHASE1
-
Insulin Therapy in the Hospital Comparing Two Protocols
NCT00841919 ·Status: COMPLETED ·Phase: PHASE4
-
A Trial to Investigate Pharmacokinetics, Pharmacodynamics, Safety and Tolerability of BioChaperone® Pramlintide Insulin in Patients With Type 1 Diabetes Mellitus
NCT03512236 ·Status: COMPLETED ·Phase: PHASE1