A Dose Ranging Study Evaluating Efficacy and Safety of NI-03 (Tactic)
Primary Purpose
Chronic Pancreatitis
Status
Completed
Phase
Phase 1
Locations
International
Study Type
Interventional
Intervention
NI-03
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Chronic Pancreatitis
Eligibility Criteria
Inclusion Criteria:
To be eligible to participate in this study, subjects must meet all of the following criteria at Screening:
- Males and females aged 18 to 85 years, inclusive, at the time of consent
- Ability to communicate effectively with clinic site staff, ability and willingness to comply with the study schedule, restrictions, and requirements
- Institutional Review Board (IRB)-approved written informed consent
- Diagnosis of chronic pancreatitis
- Baseline average daily worst pain score must be a minimum of 4 using the Numeric Rating Scale (NRS) during the 7-day run-in period
- Patients on a non-opioid analgesic regimen that is expected to remain stable during the study period, or an opioid regimen with a morphine-equivalent dose not more than 100 mg daily.
Exclusion Criteria:
To be eligible to participate in this study, subjects must not meet any of the following criteria:
- Any other clinically significant medical condition
- Treatment with any investigational product within 14 days of Day 1 (or 5 drug half-lives if 5 drug half-lives are expected to exceed 14 days) of Day -7
- Major abdominal surgery within 90 days of Day 1
- History or presence of clinically significant cardiovascular disease
- History of any cancer, except non-melanoma skin cancer, within 5 years of study enrollment,
- History of endoscopic intervention within the previous 3 months or presence of a pancreatic duct stent
- History of illicit drug abuse (i.e. use of any 'illegal' drugs within 6 months)
- Active heavy alcohol use (defined as more than 2 alcoholic drinks per day or 14 alcoholic drinks per week)
- Inadequate venous access
- Significant blood loss, donation of ≥450 mL of blood, or blood or blood product transfusion within 7 days of Day 1
- History or presence of hepatitis B (surface antigen positivity), active hepatitis C or human immunodeficiency virus (HIV) antibody
- Active infection within 30 days of Day 1
- Pregnant, planning to become pregnant or breast feeding
- Positive urine or serum pregnancy test result at Screening or on Day 1
- Active major psychiatric illness requiring a change in treatment within 3 months that would confound pain assessments
- History of seizures within the last 12 months
- Current use of anticonvulsants, antipsychotics, systemic steroids and, immunosuppressant therapy. *Use of gabapentin, pregabalin and benzodiazepines as treatment for chronic pancreatitis pain are allowed.
- Presence of generalized pain syndrome apart from chronic pancreatitis
Sites / Locations
- University of Arkansas
- Kaiser Permanente Medical Group
- University of Southern California, Keck School of Medicine
- Stanford University School of Medicine
- University of Colorado-Div of Gastroenterology and Hepatology
- Yale School of Medicine
- University of Florida - Division of Gastroenterology
- Borland-Groover Clinic
- Gastroenterology Group of Naples
- The Carle Foundation Hospital
- Indiana University - Indiana University Hospital
- University of Iowa Hospitals and Clinics
- UMass Memorial Medical Center
- Clinical Research Institute of Michigan, LLC
- Gastroenterology Associates of Western Michigan
- Kansas City Research Institute
- Dartmouth-Hitchcock Medical Center
- Columbia University School of Medicine
- PMG Research of Winston-Salem
- MetroHealth Medical Center
- Ohio State University (OSU) - Wexner Medical Center
- UPMC Presbyterian
- Medical University of South Carolina (MUSC)
- Texas Clinical Research Institute
- Texas Tech University Health Sciences Center
- Baylor College of Medicine
- Virginia Mason
- Wisconsin Center for Advanced Research, a division of GI Associates LLC
- Federal Research Centre Institute of Cytology and Genetics
- Military Medical Academu, Dep of Therapy of Adv. Training
- Military Medical Academy, Department of Hospital Therapy
- 1st Saint Petersburg State Medical University
- City Hospital #40
- City Polyclinic #4
- Medical University "Reaviz"
- Tomsk Regional Clinical Hospital
- Institute of Gastroenterology
- Central city Clinical Hospital, Therapeutic Department #2
- Malaya Therapy National Institute
- City Policlinic #9
- City Hospital Named After Tropins, Therapy Department #1
- OK Clinic
- Medical Center "Consilium Medical"
- Emergency Care Hospital, #1 Therapeutic Department
- Regional Hospital, Department of General Surgery
- 1st City Clinical Hospital, Therapeutic Department
- City Clinical Hospital #1, Gastroenterology Department
- Medical Centre Diaservis
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Placebo Comparator
Experimental
Experimental
Experimental
Arm Label
placebo
100 mg NI-03
200 mg NI-03
300 mg NI-03
Arm Description
TID Day for 28 Days
TID Day for 28 Days
TID Day for 28 Days
TID Day for 28 Days
Outcomes
Primary Outcome Measures
Phase 1 - To determine the pharmacokinetic profile for FOY251 and GBA
Pharmacokinetic (PK) parameters such as Maximum concentration (Cmax), time to maximum concentration (Tmax), minimum concentration(Cmin), area under the curve (AUC), half-life (t1/2), apparent clearance (CL/F), and apparent volume of distribution (Vz/F) are assessed.
Phase 1 - Safety and Tolerability - Treatment Emergent Adverse Events (TEAE) via CTCAE v4.0
Number of participants with treatment-related adverse events as assessed by CTCAE v4.0
Phase 1 - Safety and Tolerability - Laboratory test results
Laboratory test results will be graded and summarized based on CTCAE v4.03. and by shifts in results before and after dosing
Phase 2 - Efficacy Analysis - average daily worst pain intensity score
Secondary Outcome Measures
Phase 1 - To determine the pharmacokinetic profile for FOY251 and GBA -area under the curve (AUC)
Phase 1 - To determine the pharmacokinetic profile for FOY251 and GBA - Maximum concentration (Cmax)
Phase 1 - To determine the pharmacokinetic profile for FOY251 and GBA - time to maximum plasma concentration (tmax)
Phase 1 - To determine the pharmacokinetic profile for FOY251 and GBA - apparent clearance (CL/F)
Phase 1 - To determine the pharmacokinetic profile for FOY251 and GBA - plasma terminal half-life (t1/2)
Phase 1 - To determine the pharmacokinetic profile for FOY251 and GBA - apparent volume of distribution (Vz/F)
Phase 2 - Efficacy Analysis - Change from baseline in least pain score
Phase 2 - Efficacy Analysis - Change from baseline in average pain score
Phase 2 - Efficacy Analysis - Change from baseline in current pain score
Phase 2 - Efficacy Analysis - Change from baseline in average morphine-equivalent daily opioid daily dose
Phase 2 - Efficacy Analysis - Change from baseline in quality of life
assessed using the pain interference aspects of the Brief Pain Inventory (BPI)
Phase 2 - Safety and Tolerability - Treatment Emergent Adverse Events (TEAE) via CTCAE v4.0
Number of participants with treatment-related adverse events as assessed by CTCAE v4.0
Phase 2 - Safety and tolerability - Laboratory Test Results
Laboratory test results will be graded and summarized based on CTCAE v4.03. and by shifts in results before and after dosing
Phase 2 - To determine the pharmacokinetic profile for FOY251 and GBA -area under the curve (AUC)
Phase 2 - To determine the pharmacokinetic profile for FOY251 and GBA - Maximum concentration (Cmax)
Phase 2 - To determine the pharmacokinetic profile for FOY251 and GBA - time to maximum plasma concentration (tmax)
Phase 2 - To determine the pharmacokinetic profile for FOY251 and GBA - plasma terminal half-life (t1/2)
Phase 2 - To determine the pharmacokinetic profile for FOY251 and GBA - apparent clearance (CL/F)
Phase 2 - To determine the pharmacokinetic profile for FOY251 and GBA - apparent volume of distribution (Vz/F)
Full Information
NCT ID
NCT02693093
First Posted
February 12, 2016
Last Updated
December 14, 2022
Sponsor
Kangen Pharmaceuticals, Inc
1. Study Identification
Unique Protocol Identification Number
NCT02693093
Brief Title
A Dose Ranging Study Evaluating Efficacy and Safety of NI-03
Acronym
Tactic
Official Title
A Phase 1, Single Dose PK and Safety Study With NI-03 Followed by a Phase 2, Randomized, Double-Blind, Parallel-Group Dose-Ranging Study to Evaluate the Safety and Efficacy of NI-03 When Compared to Placebo in Subjects With Chronic Pancreatitis
Study Type
Interventional
2. Study Status
Record Verification Date
December 2022
Overall Recruitment Status
Completed
Study Start Date
February 24, 2016 (Actual)
Primary Completion Date
September 30, 2021 (Actual)
Study Completion Date
December 30, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Kangen Pharmaceuticals, Inc
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to determine the safety and efficacy of NI-03.
Detailed Description
The primary objective of the Single-Dose Phase is to assess the pharmacokinetics (PK) and safety of single doses of NI-03 when administered at doses of 100 mg, 200 mg or 300 mg to subjects with chronic pancreatitis.
The primary objective of the Double-Blind Phase of the study is to determine the efficacy, PK and safety of three doses of NI-03 (100 mg, 200 mg and 300 mg) as compared to placebo when administered three times daily (TID) for 28 consecutive days in subjects with chronic pancreatitis.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Pancreatitis
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
264 (Actual)
8. Arms, Groups, and Interventions
Arm Title
placebo
Arm Type
Placebo Comparator
Arm Description
TID Day for 28 Days
Arm Title
100 mg NI-03
Arm Type
Experimental
Arm Description
TID Day for 28 Days
Arm Title
200 mg NI-03
Arm Type
Experimental
Arm Description
TID Day for 28 Days
Arm Title
300 mg NI-03
Arm Type
Experimental
Arm Description
TID Day for 28 Days
Intervention Type
Drug
Intervention Name(s)
NI-03
Intervention Type
Drug
Intervention Name(s)
Placebo
Primary Outcome Measure Information:
Title
Phase 1 - To determine the pharmacokinetic profile for FOY251 and GBA
Description
Pharmacokinetic (PK) parameters such as Maximum concentration (Cmax), time to maximum concentration (Tmax), minimum concentration(Cmin), area under the curve (AUC), half-life (t1/2), apparent clearance (CL/F), and apparent volume of distribution (Vz/F) are assessed.
Time Frame
pre-dose and at 0.25, 0.5, 1, 2, 4 and 8 hours post-dose
Title
Phase 1 - Safety and Tolerability - Treatment Emergent Adverse Events (TEAE) via CTCAE v4.0
Description
Number of participants with treatment-related adverse events as assessed by CTCAE v4.0
Time Frame
through 7 days post-dose
Title
Phase 1 - Safety and Tolerability - Laboratory test results
Description
Laboratory test results will be graded and summarized based on CTCAE v4.03. and by shifts in results before and after dosing
Time Frame
through 7 days post-dose
Title
Phase 2 - Efficacy Analysis - average daily worst pain intensity score
Time Frame
4 Weeks
Secondary Outcome Measure Information:
Title
Phase 1 - To determine the pharmacokinetic profile for FOY251 and GBA -area under the curve (AUC)
Time Frame
pre-dose and at 0.25, 0.5, 1, 2, 4 and 8 hours post-dose.
Title
Phase 1 - To determine the pharmacokinetic profile for FOY251 and GBA - Maximum concentration (Cmax)
Time Frame
pre-dose and at 0.25, 0.5, 1, 2, 4 and 8 hours post-dose.
Title
Phase 1 - To determine the pharmacokinetic profile for FOY251 and GBA - time to maximum plasma concentration (tmax)
Time Frame
pre-dose and at 0.25, 0.5, 1, 2, 4 and 8 hours post-dose.
Title
Phase 1 - To determine the pharmacokinetic profile for FOY251 and GBA - apparent clearance (CL/F)
Time Frame
pre-dose and at 0.25, 0.5, 1, 2, 4 and 8 hours post-dose.
Title
Phase 1 - To determine the pharmacokinetic profile for FOY251 and GBA - plasma terminal half-life (t1/2)
Time Frame
pre-dose and at 0.25, 0.5, 1, 2, 4 and 8 hours post-dose.
Title
Phase 1 - To determine the pharmacokinetic profile for FOY251 and GBA - apparent volume of distribution (Vz/F)
Time Frame
pre-dose and at 0.25, 0.5, 1, 2, 4 and 8 hours post-dose.
Title
Phase 2 - Efficacy Analysis - Change from baseline in least pain score
Time Frame
change from baseline to Week 4
Title
Phase 2 - Efficacy Analysis - Change from baseline in average pain score
Time Frame
4 Weeks
Title
Phase 2 - Efficacy Analysis - Change from baseline in current pain score
Time Frame
4 Weeks
Title
Phase 2 - Efficacy Analysis - Change from baseline in average morphine-equivalent daily opioid daily dose
Time Frame
4 Weeks
Title
Phase 2 - Efficacy Analysis - Change from baseline in quality of life
Description
assessed using the pain interference aspects of the Brief Pain Inventory (BPI)
Time Frame
change from baseline to Week 4
Title
Phase 2 - Safety and Tolerability - Treatment Emergent Adverse Events (TEAE) via CTCAE v4.0
Description
Number of participants with treatment-related adverse events as assessed by CTCAE v4.0
Time Frame
Through day 57 (End of Study Visit)
Title
Phase 2 - Safety and tolerability - Laboratory Test Results
Description
Laboratory test results will be graded and summarized based on CTCAE v4.03. and by shifts in results before and after dosing
Time Frame
Through day 57 (End of Study Visit)
Title
Phase 2 - To determine the pharmacokinetic profile for FOY251 and GBA -area under the curve (AUC)
Time Frame
Days 1 and 29, and at 0.25, 0.5, 1, 2 and 4 hours post-dose
Title
Phase 2 - To determine the pharmacokinetic profile for FOY251 and GBA - Maximum concentration (Cmax)
Time Frame
pre-dose and at 0.25, 0.5, 1, 2, 4 and 8 hours post-dose.
Title
Phase 2 - To determine the pharmacokinetic profile for FOY251 and GBA - time to maximum plasma concentration (tmax)
Time Frame
Days 1 and 29, and at 0.25, 0.5, 1, 2 and 4 hours post-dose
Title
Phase 2 - To determine the pharmacokinetic profile for FOY251 and GBA - plasma terminal half-life (t1/2)
Time Frame
Days 1 and 29, and at 0.25, 0.5, 1, 2 and 4 hours post-dose
Title
Phase 2 - To determine the pharmacokinetic profile for FOY251 and GBA - apparent clearance (CL/F)
Time Frame
Days 1 and 29, and at 0.25, 0.5, 1, 2 and 4 hours post-dose
Title
Phase 2 - To determine the pharmacokinetic profile for FOY251 and GBA - apparent volume of distribution (Vz/F)
Time Frame
Days 1 and 29, and at 0.25, 0.5, 1, 2 and 4 hours post-dose
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
To be eligible to participate in this study, subjects must meet all of the following criteria at Screening:
Males and females aged 18 to 85 years, inclusive, at the time of consent
Ability to communicate effectively with clinic site staff, ability and willingness to comply with the study schedule, restrictions, and requirements
Institutional Review Board (IRB)-approved written informed consent
Diagnosis of chronic pancreatitis
Baseline average daily worst pain score must be a minimum of 4 using the Numeric Rating Scale (NRS) during the 7-day run-in period
Patients on a non-opioid analgesic regimen that is expected to remain stable during the study period, or an opioid regimen with a morphine-equivalent dose not more than 100 mg daily.
Exclusion Criteria:
To be eligible to participate in this study, subjects must not meet any of the following criteria:
Any other clinically significant medical condition
Treatment with any investigational product within 14 days of Day 1 (or 5 drug half-lives if 5 drug half-lives are expected to exceed 14 days) of Day -7
Major abdominal surgery within 90 days of Day 1
History or presence of clinically significant cardiovascular disease
History of any cancer, except non-melanoma skin cancer, within 5 years of study enrollment,
History of endoscopic intervention within the previous 3 months or presence of a pancreatic duct stent
History of illicit drug abuse (i.e. use of any 'illegal' drugs within 6 months)
Active heavy alcohol use (defined as more than 2 alcoholic drinks per day or 14 alcoholic drinks per week)
Inadequate venous access
Significant blood loss, donation of ≥450 mL of blood, or blood or blood product transfusion within 7 days of Day 1
History or presence of hepatitis B (surface antigen positivity), active hepatitis C or human immunodeficiency virus (HIV) antibody
Active infection within 30 days of Day 1
Pregnant, planning to become pregnant or breast feeding
Positive urine or serum pregnancy test result at Screening or on Day 1
Active major psychiatric illness requiring a change in treatment within 3 months that would confound pain assessments
History of seizures within the last 12 months
Current use of anticonvulsants, antipsychotics, systemic steroids and, immunosuppressant therapy. *Use of gabapentin, pregabalin and benzodiazepines as treatment for chronic pancreatitis pain are allowed.
Presence of generalized pain syndrome apart from chronic pancreatitis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Phiip Hart, MD
Organizational Affiliation
OSU
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Arkansas
City
Little Rock
State/Province
Arkansas
ZIP/Postal Code
72204
Country
United States
Facility Name
Kaiser Permanente Medical Group
City
Los Angeles
State/Province
California
ZIP/Postal Code
90027
Country
United States
Facility Name
University of Southern California, Keck School of Medicine
City
Los Angeles
State/Province
California
ZIP/Postal Code
90033
Country
United States
Facility Name
Stanford University School of Medicine
City
Stanford
State/Province
California
ZIP/Postal Code
94305
Country
United States
Facility Name
University of Colorado-Div of Gastroenterology and Hepatology
City
Aurora
State/Province
Colorado
ZIP/Postal Code
80045
Country
United States
Facility Name
Yale School of Medicine
City
New Haven
State/Province
Connecticut
ZIP/Postal Code
06519
Country
United States
Facility Name
University of Florida - Division of Gastroenterology
City
Gainesville
State/Province
Florida
ZIP/Postal Code
32608
Country
United States
Facility Name
Borland-Groover Clinic
City
Jacksonville
State/Province
Florida
ZIP/Postal Code
32256
Country
United States
Facility Name
Gastroenterology Group of Naples
City
Naples
State/Province
Florida
ZIP/Postal Code
34102
Country
United States
Facility Name
The Carle Foundation Hospital
City
Urbana
State/Province
Illinois
ZIP/Postal Code
61801
Country
United States
Facility Name
Indiana University - Indiana University Hospital
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46202-5149
Country
United States
Facility Name
University of Iowa Hospitals and Clinics
City
Iowa City
State/Province
Iowa
ZIP/Postal Code
52242
Country
United States
Facility Name
UMass Memorial Medical Center
City
Worcester
State/Province
Massachusetts
ZIP/Postal Code
01605
Country
United States
Facility Name
Clinical Research Institute of Michigan, LLC
City
Chesterfield
State/Province
Michigan
ZIP/Postal Code
48047
Country
United States
Facility Name
Gastroenterology Associates of Western Michigan
City
Wyoming
State/Province
Michigan
ZIP/Postal Code
49519
Country
United States
Facility Name
Kansas City Research Institute
City
Kansas City
State/Province
Missouri
ZIP/Postal Code
64131
Country
United States
Facility Name
Dartmouth-Hitchcock Medical Center
City
Lebanon
State/Province
New Hampshire
ZIP/Postal Code
03756
Country
United States
Facility Name
Columbia University School of Medicine
City
New York
State/Province
New York
ZIP/Postal Code
10027
Country
United States
Facility Name
PMG Research of Winston-Salem
City
Winston-Salem
State/Province
North Carolina
ZIP/Postal Code
27103
Country
United States
Facility Name
MetroHealth Medical Center
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44109
Country
United States
Facility Name
Ohio State University (OSU) - Wexner Medical Center
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43210
Country
United States
Facility Name
UPMC Presbyterian
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213-2536
Country
United States
Facility Name
Medical University of South Carolina (MUSC)
City
Charleston
State/Province
South Carolina
ZIP/Postal Code
29425
Country
United States
Facility Name
Texas Clinical Research Institute
City
Arlington
State/Province
Texas
ZIP/Postal Code
76012
Country
United States
Facility Name
Texas Tech University Health Sciences Center
City
El Paso
State/Province
Texas
ZIP/Postal Code
79905
Country
United States
Facility Name
Baylor College of Medicine
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Facility Name
Virginia Mason
City
Seattle
State/Province
Washington
ZIP/Postal Code
98101
Country
United States
Facility Name
Wisconsin Center for Advanced Research, a division of GI Associates LLC
City
Milwaukee
State/Province
Wisconsin
ZIP/Postal Code
53215
Country
United States
Facility Name
Federal Research Centre Institute of Cytology and Genetics
City
Novosibirsk
ZIP/Postal Code
630089
Country
Russian Federation
Facility Name
Military Medical Academu, Dep of Therapy of Adv. Training
City
Saint Petersburg
ZIP/Postal Code
191015
Country
Russian Federation
Facility Name
Military Medical Academy, Department of Hospital Therapy
City
Saint Petersburg
ZIP/Postal Code
191124
Country
Russian Federation
Facility Name
1st Saint Petersburg State Medical University
City
Saint Petersburg
ZIP/Postal Code
197022
Country
Russian Federation
Facility Name
City Hospital #40
City
Saint Petersburg
ZIP/Postal Code
197706
Country
Russian Federation
Facility Name
City Polyclinic #4
City
Saint Petersburg
ZIP/Postal Code
199178
Country
Russian Federation
Facility Name
Medical University "Reaviz"
City
Samara
ZIP/Postal Code
443011
Country
Russian Federation
Facility Name
Tomsk Regional Clinical Hospital
City
Tomsk
ZIP/Postal Code
634063
Country
Russian Federation
Facility Name
Institute of Gastroenterology
City
Dnipro
ZIP/Postal Code
49074
Country
Ukraine
Facility Name
Central city Clinical Hospital, Therapeutic Department #2
City
Ivano-Frankivsk
ZIP/Postal Code
76018
Country
Ukraine
Facility Name
Malaya Therapy National Institute
City
Kharkiv
ZIP/Postal Code
61039
Country
Ukraine
Facility Name
City Policlinic #9
City
Kharkiv
ZIP/Postal Code
61172
Country
Ukraine
Facility Name
City Hospital Named After Tropins, Therapy Department #1
City
Kherson
ZIP/Postal Code
73000
Country
Ukraine
Facility Name
OK Clinic
City
Kyiv
ZIP/Postal Code
02091
Country
Ukraine
Facility Name
Medical Center "Consilium Medical"
City
Kyiv
ZIP/Postal Code
04050
Country
Ukraine
Facility Name
Emergency Care Hospital, #1 Therapeutic Department
City
Lviv
ZIP/Postal Code
79059
Country
Ukraine
Facility Name
Regional Hospital, Department of General Surgery
City
Odesa
ZIP/Postal Code
65025
Country
Ukraine
Facility Name
1st City Clinical Hospital, Therapeutic Department
City
Poltava
ZIP/Postal Code
36038
Country
Ukraine
Facility Name
City Clinical Hospital #1, Gastroenterology Department
City
Vinnytsia
ZIP/Postal Code
21029
Country
Ukraine
Facility Name
Medical Centre Diaservis
City
Zaporizhia
ZIP/Postal Code
69076
Country
Ukraine
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
31412955
Citation
Ramsey ML, Nuttall J, Hart PA; TACTIC Investigative Team. A phase 1/2 trial to evaluate the pharmacokinetics, safety, and efficacy of NI-03 in patients with chronic pancreatitis: study protocol for a randomized controlled trial on the assessment of camostat treatment in chronic pancreatitis (TACTIC). Trials. 2019 Aug 14;20(1):501. doi: 10.1186/s13063-019-3606-y.
Results Reference
derived
Learn more about this trial
A Dose Ranging Study Evaluating Efficacy and Safety of NI-03
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