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Clinical Trials/NCT03847207
NCT03847207
Completed
Phase 1

A Three-Part Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single Ascending Subcutaneous Doses of HTL0030310 in Healthy Subjects

Nxera Pharma UK Limited1 site in 1 country42 target enrollmentJanuary 23, 2019

Overview

Phase
Phase 1
Intervention
HTL0030310
Conditions
Healthy
Sponsor
Nxera Pharma UK Limited
Enrollment
42
Locations
1
Primary Endpoint
Part 2 and Part 3 Maximum observed effect (EMax) 1) for insulin, glucose, glucagon, GLP1, C-peptide and GIP level 2) for GH 3) ACTH and cortisol
Status
Completed
Last Updated
last year

Overview

Brief Summary

A Phase 1, first in human, three-part, single centre study to assess the safety, tolerability, PK and PD of single ascending subcutaneous doses of HTL0030310 in healthy subjects

Detailed Description

This is a first in human, three part study with the objective to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of single ascending subcutaneous doses of HTL0030310 in healthy subjects. Part 1 is a double-blind, placebo-controlled, randomised study assessing single ascending doses of HTL0030310. Part 2 is a site-blind (sponsor unblinded), placebo-controlled, part-randomised, fixed-sequence, single-dose, 4-period study assessing the PD of a positive control, pasireotide, following administration of challenge agents. Part 3 is a double-blind, placebo-controlled, part-randomised, fixed-sequence, single-dose, HTL0030310 proof of pharmacological effect study, where PD effects of HTL0030310 will be investigated following administration of challenge agents. The challenge agents administered in this study will be: oral glucose tolerance test (OGTT), Growth hormone-releasing hormone (GHRH), and corticotrophin releasing hormone (CRH) combined with desmopressin.

Registry
clinicaltrials.gov
Start Date
January 23, 2019
End Date
March 5, 2020
Last Updated
last year
Study Type
Interventional
Study Design
Sequential
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Arms & Interventions

Part 1 Single Ascending Dose

Eight subjects in up to 8 cohorts will be dosed. A single subcutaneous injection of HTL0030310 or placebo will be administered. In each cohort, 6 subjects will receive HTL0030310 and 2 subjects will receive placebo.

Intervention: HTL0030310

Part 1 Single Ascending Dose

Eight subjects in up to 8 cohorts will be dosed. A single subcutaneous injection of HTL0030310 or placebo will be administered. In each cohort, 6 subjects will receive HTL0030310 and 2 subjects will receive placebo.

Intervention: Placebo

Part 2 Pasireotide PD Assessment

Sixteen subjects in 2 cohorts (8 subjects per cohort) will be dosed on 4 occasions. Within each cohort, 4 subjects will be randomised to active dosing with CRH with desmopressin, GHRH and OGTT challenge and 4 subjects will be randomised to placebo dosing with CRH with desmopressin, GHRH and OGTT challenge.

Intervention: Pasireotide

Part 2 Pasireotide PD Assessment

Sixteen subjects in 2 cohorts (8 subjects per cohort) will be dosed on 4 occasions. Within each cohort, 4 subjects will be randomised to active dosing with CRH with desmopressin, GHRH and OGTT challenge and 4 subjects will be randomised to placebo dosing with CRH with desmopressin, GHRH and OGTT challenge.

Intervention: Placebo

Part 3 Proof of Pharmacological Effect

Up to 80 subjects in 4 cohorts (up to 20 subjects per cohort) will be dosed in up to 3 study periods. In each period, subjects will receive active drug or placebo with GHRH, OGTT and CRH with desmopressin (optional).

Intervention: HTL0030310

Part 3 Proof of Pharmacological Effect

Up to 80 subjects in 4 cohorts (up to 20 subjects per cohort) will be dosed in up to 3 study periods. In each period, subjects will receive active drug or placebo with GHRH, OGTT and CRH with desmopressin (optional).

Intervention: Placebo

Outcomes

Primary Outcomes

Part 2 and Part 3 Maximum observed effect (EMax) 1) for insulin, glucose, glucagon, GLP1, C-peptide and GIP level 2) for GH 3) ACTH and cortisol

Time Frame: Predose up to 4 hours post dose

Pharmacodynamics

Part 1: Number of treatment related adverse events (as determined by abnormal clinical laboratory tests, vitals signs, ECG parameters, Holter ECG parameters and injection site reactions)

Time Frame: Admission up to 8 days post dose

Safety and Tolerability

Part 2 and Part 3 Area under the effect time curve (EAUC) 1) for insulin, glucose, glucagon, GLP1, C-peptide and GIP level 2) for GH 3) ACTH and cortisol

Time Frame: Predose up to 4 hours post dose

Pharmacodynamics

Part 2 and Part 3 Time to reach Maximum observed effect (TEMax) 1) for insulin, glucose, glucagon, GLP1, C-peptide and GIP level 2) for GH 3) ACTH and cortisol

Time Frame: Predose up to 4 hours post dose

Pharmacodynamics

Secondary Outcomes

  • Part 2 Time to reach Maximum observed plasma concentration (Tmax) of single subcutaneous doses of pasireotide(Predose to 24 hours postdose)
  • Part 1 Area under the curve (AUC) of single subcutaneous doses of HTL0030310(Pre dose to 144 hours post dose)
  • Part 3 Time to reach Maximum observed plasma concentration (Tmax) of single subcutaneous doses of HTL0030310(Predose to 96 hours postdose)
  • Part 3 Area under the curve (AUC) of single subcutaneous doses of HTL0030310(Predose to 96 hours postdose)
  • Part 1 Maximum observed plasma concentration (Cmax) of single subcutaneous doses of HTL0030310(Pre dose to 144 hours post dose)
  • Part 1 Time to reach Maximum observed plasma concentration (Tmax) of single subcutaneous doses of HTL0030310(Pre dose to 144 hours post dose)
  • Part 2 Maximum observed plasma concentration (Cmax) of single subcutaneous doses of pasireotide(Predose to 24 hours postdose)
  • Part 3: Number of treatment related adverse events (as determined by abnormal clinical laboratory tests, vitals signs, ECG parameters and injection site reactions)(Admission up to 8 to 10 days post final dose)
  • Part 2 Area under the curve (AUC) of single subcutaneous doses of pasireotide(Predose to 24 hours postdose)
  • Part 3 Maximum observed plasma concentration (Cmax) of single subcutaneous doses of HTL0030310(Predose to 96 hours postdose)

Study Sites (1)

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