- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04903873
A Study to Evaluate Safety, Efficacy, and Pharmacokinetics in Participants With Advanced Solid Tumors
March 13, 2024 updated by: Eutilex
An Open-Label, Phase 1/2 Study to Evaluate Safety, Efficacy, and Pharmacokinetics of EU101, an Agonistic Anti-CD137 (4-1BB) Monoclonal Antibody in Patients With Advanced Solid Tumors
Phase 1 (Dose Escalation) of this study will assess the safety, tolerability, dose-limiting toxicity (DLT), and will determine the maximum tolerated dose (MTD) and recommended Phase 2 dose (RP2D) of EU101 in participants with advanced solid tumors.
Phase 2 (Dose Expansion) of the study will assess the antitumor effect of EU101 in two indications including colorectal cancer (CRC) and non-small cell lung cancer (NSCLC).
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
110
Phase
- Phase 2
- Phase 1
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Seoyoun Kim, MPH
- Phone Number: 82-10-4227-0925
- Email: s.kim@eutilex.com
Study Locations
-
-
-
Ilsan, Korea, Republic of
- Not yet recruiting
- National Cancer Center
-
Contact:
- Tak Yun, MD, PhD
-
Sub-Investigator:
- Tak Yun, MD, PhD
-
Sub-Investigator:
- Won-Young Choi, MD, PhD
-
Seoul, Korea, Republic of
- Recruiting
- Severance Hospital
-
Contact:
- Hye Ryun Kim, MD
-
Sub-Investigator:
- Min Hee Hong, MD
-
Sub-Investigator:
- Chang Gon Kim, MD
-
Sub-Investigator:
- Seung-Hoon Beom, MD
-
Sub-Investigator:
- SANG JOON SHIN, MD
-
Sub-Investigator:
- Min Hwan Kim, MD
-
Sub-Investigator:
- Gun Min Kim, MD
-
Sub-Investigator:
- Han Sang Kim, MD
-
Sub-Investigator:
- Choong-kun Lee, MD
-
Seoul, Korea, Republic of
- Recruiting
- Samsung Seoul Hospital
-
Contact:
- Myung-Ju Ahn, MD, PhD
-
Sub-Investigator:
- Jong-Mu Sun, MD, PhD
-
Sub-Investigator:
- Jin-Seok Ahn, MD, PhD
-
Sub-Investigator:
- Hyun-Ae Jung, MD, PhD
-
Sub-Investigator:
- Se-Hoon Lee, MD, PhD
-
Sub-Investigator:
- Ji-Yun Lee, MD, PhD
-
Sub-Investigator:
- Seh-Hoon Park, MD, PhD
-
Seoul, Korea, Republic of
- Recruiting
- Seoul Asan
-
Contact:
- Tae Won Kim, MD, PhD
-
Sub-Investigator:
- Jae-Ho Jeong, MD, PhD
-
Sub-Investigator:
- Sang-We Kim, MD, PhD
-
Sub-Investigator:
- Jeong-Eun Kim, MD, PhD
-
Sub-Investigator:
- Hyung-Don Kim, MD, PhD
-
Sub-Investigator:
- Dae-Ho Lee, MD, PhD
-
Sub-Investigator:
- Se-Young Seo, MD, PhD
-
Sub-Investigator:
- Shin-Kyo Yoon, MD, PhD
-
Sub-Investigator:
- Yong-Sang Hong, MD, PhD
-
-
-
-
Pennsylvania
-
Philadelphia, Pennsylvania, United States, 19111
- Recruiting
- Fox Chase Cancer Center
-
Contact:
- Anthony Olszanski, MD
-
Sub-Investigator:
- Igor Astsaturov, MD
-
Sub-Investigator:
- Efrat Dotan, MD
-
Sub-Investigator:
- Angela Jain, MD
-
Sub-Investigator:
- Jessica Bauman, MD
-
Sub-Investigator:
- Daniel Geynisman, MD
-
Sub-Investigator:
- Elizabeth Pilmack, MD
-
Sub-Investigator:
- Joseph Bodor, MD
-
Sub-Investigator:
- Anshu Giri, MD
-
Sub-Investigator:
- Matthew Zibelman, MD
-
-
Texas
-
Dallas, Texas, United States, 75230
- Recruiting
- Mary Crowley Center
-
Sub-Investigator:
- Jairo Olivares, MD
-
Sub-Investigator:
- James Strauss, MD
-
Sub-Investigator:
- Ntombizodwa Sayi, MD
-
Sub-Investigator:
- Leah Plato, MD
-
Sub-Investigator:
- Jennifer Ashun, MD
-
Sub-Investigator:
- Douglas Orr, MD
-
Sub-Investigator:
- Reva Schnieder, MD
-
Contact:
- Minal Barve, MD
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Description
Key Inclusion Criteria:
- Histologically or cytologically confirmed diagnosis of metastatic or locally advanced solid tumors for which no standard therapy exists or standard therapy has failed because of disease progression or unacceptable toxicities. Also includes patients who cannot be treated with standard therapy because of underlying/existing medical condition.
- Cohort 1 (colorectal cancer): a) CRC (including microsatellite instability-high [MSI-H] and microsatellite-stable [MSS]) regardless of RAS mutation. b) Disease progression within 3 months after last administration of approved standard therapies. c) Prior cytotoxic chemotherapy for metastatic disease include all the following agents: fluoropyrimidine, oxaliplatin, and irinotecan
- Adjuvant chemotherapy-based treatments count as prior therapy, as long as relapse had occurred within 6 months of completion of such therapies, prior anti-epidermal growth factor receptor (EGFR) therapy (cetuximab, panitumumab), anti-angiogenic therapy (bevacizumab, aflibercept, ramucirumab), regorafenib, and TAS-102 are allowed. d) No more than 5 prior therapies for metastatic disease. For participants who had disease recurrence within 6 months of completing adjuvant chemotherapy, the adjuvant regimen can be considered as 1 chemotherapy regimen for metastatic disease
- Cohort 2 (NSCLC): a) NSCLC without known EGFR, anaplastic lymphoma kinase (ALK), and ROS1 genomic tumor aberrations. b) No standard therapy exists or standard therapy has failed. c) No more than 3 prior therapies for metastatic disease
- Phase 2: At least 1 measurable lesion per RECIST version 1.1
- Eastern Cooperative Oncology Group (ECOG) performance score of 0 to 2
- Adequate organ and bone marrow function (Hemoglobin >9.0 g/dL, Absolute neutrophil count ≥1,500/μL, Absolute lymphocyte count ≥600 and ≤2,500/μL, Platelet count ≥100,000/μL, Total bilirubin ≤1.5 × upper limit of normal, Alanine aminotransferase and aspartate aminotransferase ≤2.5 × ULN, Serum creatinine ≤1.5 × ULN or creatinine clearance >30 mL/min, Prothrombin time and activated partial thromboplastin time ≤1.5 × ULN)
- Life expectancy of at least 12 weeks
- Voluntarily provided a written consent to participate in the study
- Women of childbearing potential (WOCBP) must have a negative serum pregnancy test within the 7 days before study drug administration
- WOCBP and sexually active fertile male patients with partners who are WOCBP must agree to use 2 highly effective methods of contraception throughout the course of the study and for 12 weeks after the last dose of study drug.
Key Exclusion Criteria:
- Primary central nervous system (CNS) tumor (Phase 1), CNS metastasis, and/or carcinomatous meningitis. Participants with prior brain metastases treated at least 4 weeks before the first dose of EU101 that are clinically stable and do not require chronic corticosteroid treatment are allowed. Untreated but asymptomatic and clinically stable brain metastases per investigator's discretion are allowed
- Received prior therapy with any anti-CD137 monoclonal antibody (mAb) or agent
- Major surgery requiring general anesthesia within 3 weeks before first dose of EU101 or still recovering from prior surgery
- Active infection that is not controlled or requires intravenous antibiotics in the last 2 weeks
- History of allogeneic tissue or organ transplant
- Active hepatitis B virus or hepatitis C virus infection
- History of any noninfectious hepatitis
- Human immunodeficiency virus (HIV) infection
- Received or receiving systemic corticosteroid therapy or any other form of systemic immunosuppressive medicaion 1 week before first dose of EU101
- Known severe (≥Grade 3) hypersensitivity reactions to antibody, or severe reaction to immuno-oncology agents requiring treatment with steroids
- Konwn or suspected hypersensitivity to EU101 or any component of its formulation
- Current or history of interstitial lung disease, anaphylaxis, uncontrolled asthma, or pneumonitis that has required systemic corticosteroids
- Patients with second primary cancer
- Clinically significant concurrent cardiovascular disease
- Pregnant women, breasfeeding women, WOCBP, or men with partners who are WOCBP who do not agree to use adequate contraceptive measures
- Determined as unable to participate in the study per investigator's judgment
Other protocol defined Inclusion/Exclusion criteria may apply
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Sequential Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: EU101: Dose Escalation Cohort
Participants with advanced solid tumors will receive EU101 intravenously once every 3 weeks (3 weeks = 1 cycle) with escalating doses starting from 0.05 milligrams per kilogram (mg/kg) to 10 mg/kg until disease progression, unacceptable toxicities or death, withdrawal of consent, end of study, or physician's decision, whichever occurs first.
|
EU101 will be administered via intravenous infusion.
|
Experimental: EU101: Dose Expansion Cohort 1
Participants with CRC will receive EU101 intravenously once every 3 weeks (3 weeks = 1 cycle) with a determined recommended phase 2 dose until disease progression, unacceptable toxicities or death, withdrawal of consent, end of study, or physician's decision, whichever occurs first.
|
EU101 will be administered via intravenous infusion.
|
Experimental: EU101: Dose Expansion Cohort 2
Participants with NSCLC will receive EU101 intravenously once every 3 weeks (3 weeks = 1 cycle) with a determined recommended phase 2 dose until disease progression, unacceptable toxicities or death, withdrawal of consent, end of study, or physician's decision, whichever occurs first.
|
EU101 will be administered via intravenous infusion.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Phase 1: Number of Participants With Adverse Event (AEs) and Serious Adverse Events (SAEs) and Adverse Events Leading to Discontinuation
Time Frame: Baseline up to 30 months
|
Baseline up to 30 months
|
|
Phase 1: Number of Participants With Dose Limiting Toxicity (DLT)
Time Frame: At the end of Cycle 1 (Each cycle is of 21 Days)
|
At the end of Cycle 1 (Each cycle is of 21 Days)
|
|
Phase 1: Number of Participants With Clinically Significant Abnormalities in Laboratory Parameters
Time Frame: Baseline up to 24 months
|
Laboratory assessments include hematology, serum chemistry, other blood tests, coagulation, and urine analysis.
Number of participants with clinically significant abnormalities will be reported.
|
Baseline up to 24 months
|
Phase 1: Number of Participants With Clinically Significant Abnormalities in Vital Signs
Time Frame: Baseline up to 24 months
|
Vital signs will include body temperature, pulse rate, and systolic and diastolic blood pressure measurements.
Number of participants with clinically significant abnormalities will be reported.
|
Baseline up to 24 months
|
Phase 1: Number of Participants With Clinically Significant Abnormalities in Physical Examination
Time Frame: Baseline up to 24 months
|
Physical examination will include head, eyes, ears, nose and throat; heart; lungs; abdomen; skin; cervical and axillary lymph nodes; and neurological and musculoskeletal systems.
Number of participants with clinically significant abnormalities will be reported.
|
Baseline up to 24 months
|
Phase 1: Number of Participants With Clinically Significant Abnormalities in 12-lead Electrocardiogram (ECG)
Time Frame: Baseline up to 24 months
|
ECG parameters included heart rhythm, pulse rate intervals, QRS, QT intervals, RR intervals and corrected QT(QTc) intervals.
Number of participants with clinically significant abnormalities will be reported.
|
Baseline up to 24 months
|
Phase 2: Objective Response Rate (ORR)
Time Frame: Time from first dose of study treatment assessed until disease progression, death, withdrawal of consent, physician's decision, start of new anticancer therapy, or end of study, whichever occurs first (approximately for 24 months)
|
Objective response rate (ORR), defined as the percentage of participants with a best overall response (BOR) of either a complete response (CR) or partial response (PR), per Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 for solid tumors by investigators.
|
Time from first dose of study treatment assessed until disease progression, death, withdrawal of consent, physician's decision, start of new anticancer therapy, or end of study, whichever occurs first (approximately for 24 months)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Phase 1: Objective Response Rate (ORR)
Time Frame: Time from first dose of study treatment assessed until disease progression, death, withdrawal of consent, physician's decision, start of new anticancer therapy, or end of study, whichever occurs first (approximately for 24 months)
|
Objective response rate (ORR), defined as the percentage of participants with a BOR of either a complete response (CR) or partial response (PR), per RECIST version 1.1 for solid tumors by investigators.
|
Time from first dose of study treatment assessed until disease progression, death, withdrawal of consent, physician's decision, start of new anticancer therapy, or end of study, whichever occurs first (approximately for 24 months)
|
Phase 1 and 2: Duration of Response (DOR)
Time Frame: Time from first dose of study treatment assessed until disease progression, death, withdrawal of consent, physician's decision, start of new anticancer therapy, or end of study, whichever occurs first (approximately for 56 months)
|
Time from first dose of study treatment assessed until disease progression, death, withdrawal of consent, physician's decision, start of new anticancer therapy, or end of study, whichever occurs first (approximately for 56 months)
|
|
Phase 1 and 2: Disease Control Rate (DCR)
Time Frame: Time from first dose of study treatment assessed until disease progression, death, withdrawal of consent, physician's decision, start of new anticancer therapy, or end of study, whichever occurs first (approximately for 56 months)
|
DCR will be defined similarly to ORR but also including stable disease (SD) in the categorization of response (i.e,
RECIST response of either CR, PR, or SD).
|
Time from first dose of study treatment assessed until disease progression, death, withdrawal of consent, physician's decision, start of new anticancer therapy, or end of study, whichever occurs first (approximately for 56 months)
|
Phase 1 and 2: Time to Response (TTR)
Time Frame: Time from first dose of study treatment assessed until disease progression, death, withdrawal of consent, physician's decision, start of new anticancer therapy, or end of study, whichever occurs first (approximately for 56 months)
|
Time from first dose of study treatment assessed until disease progression, death, withdrawal of consent, physician's decision, start of new anticancer therapy, or end of study, whichever occurs first (approximately for 56 months)
|
|
Phase 1 and 2: Time to Progression (TTP)
Time Frame: Time from first dose of study treatment assessed until disease progression, death, withdrawal of consent, physician's decision, start of new anticancer therapy, or end of study, whichever occurs first (approximately for 56 months)
|
Time from first dose of study treatment assessed until disease progression, death, withdrawal of consent, physician's decision, start of new anticancer therapy, or end of study, whichever occurs first (approximately for 56 months)
|
|
Phase 1 and 2: Durable Clinical Benefit (DCB)
Time Frame: Time from first dose of study treatment assessed until disease progression, death, withdrawal of consent, physician's decision, start of new anticancer therapy, or end of study, whichever occurs first (approximately for 56 months)
|
DCB will be defined similarly to DCR but additionally specifying that the disease control be achieved for at least 12 weeks consecutive (i.e,
RECIST response of CR, PR or SD for greater than or equal to [>=] 12 weeks consecutive).
|
Time from first dose of study treatment assessed until disease progression, death, withdrawal of consent, physician's decision, start of new anticancer therapy, or end of study, whichever occurs first (approximately for 56 months)
|
Phase 1 and 2: Progression-Free Survival (PFS)
Time Frame: Time from first dose of study treatment assessed until disease progression, death, withdrawal of consent, physician's decision, start of new anticancer therapy, or end of study, whichever occurs first (approximately for 56 months)
|
Time from first dose of study treatment assessed until disease progression, death, withdrawal of consent, physician's decision, start of new anticancer therapy, or end of study, whichever occurs first (approximately for 56 months)
|
|
Phase 1 and 2: Overall survival (OS)
Time Frame: Time from first dose of study treatment assessed until disease progression, death, withdrawal of consent, physician's decision, start of new anticancer therapy, or end of study, whichever occurs first (approximately for 56 months)
|
Time from first dose of study treatment assessed until disease progression, death, withdrawal of consent, physician's decision, start of new anticancer therapy, or end of study, whichever occurs first (approximately for 56 months)
|
|
Phase 1 and 2: Maximum Observed Serum Concentration (Cmax) of EU101
Time Frame: Cycle 1: Pre-dose up to 336 hours post-dose; Cycle 2: 504 hours post-dose; Cycle 3: Pre-dose (Each cycle is of 21 days)]
|
Cmax is defined as maximum observed serum concentration.
|
Cycle 1: Pre-dose up to 336 hours post-dose; Cycle 2: 504 hours post-dose; Cycle 3: Pre-dose (Each cycle is of 21 days)]
|
Phase 1 and 2: Trough Serum Concentration (Ctrough) of EU101
Time Frame: Cycle 1: Pre-dose up to 336 hours post-dose; Cycle 2: 504 hours post-dose; Cycle 3: Pre-dose (Each cycle is of 21 days)]
|
Ctrough is steady-state pre-dose concentration.
|
Cycle 1: Pre-dose up to 336 hours post-dose; Cycle 2: 504 hours post-dose; Cycle 3: Pre-dose (Each cycle is of 21 days)]
|
Phase 1 and 2: Time to Reach Maximum Observed Serum Concentration (Tmax) of EU101
Time Frame: Cycle 1: Pre-dose up to 336 hours post-dose; Cycle 2: 504 hours post-dose; Cycle 3: Pre-dose (Each cycle is of 21 days)]
|
Tmax is defined as time to reach maximum observed serum concentration.
|
Cycle 1: Pre-dose up to 336 hours post-dose; Cycle 2: 504 hours post-dose; Cycle 3: Pre-dose (Each cycle is of 21 days)]
|
Phase 1 and 2: Area Under the Serum Concentration-Time Curve From Time Zero to 24 Hours Post-dose (AUC0-24) of EU101
Time Frame: Cycle 1: Pre-dose up to 336 hours post-dose; Cycle 2: 504 hours post-dose; Cycle 3: Pre-dose (Each cycle is of 21 days)]
|
AUC0-24 is defined as the area under the serum concentration versus time curve from time zero (pre-dose) to 24 hours post-dose (0 to 24).
|
Cycle 1: Pre-dose up to 336 hours post-dose; Cycle 2: 504 hours post-dose; Cycle 3: Pre-dose (Each cycle is of 21 days)]
|
Phase 1 and 2: Area Under the Serum Concentration-Time Curve From Time Zero to the Last Measurable Concentration (AUC0-last) of EU101
Time Frame: Cycle 1: Pre-dose up to 336 hours post-dose; Cycle 2: 504 hours post-dose; Cycle 3: Pre-dose (Each cycle is of 21 days)]
|
AUC0-last is defined as area under the serum concentration time-curve from time zero to the time of last measured concentration.
|
Cycle 1: Pre-dose up to 336 hours post-dose; Cycle 2: 504 hours post-dose; Cycle 3: Pre-dose (Each cycle is of 21 days)]
|
Phase 1 and 2: Area Under the Serum Concentration-Time Curve From Time Zero Extrapolated to Infinity (AUC0-inf) of EU101
Time Frame: Cycle 1: Pre-dose up to 336 hours post-dose; Cycle 2: 504 hours post-dose; Cycle 3: Pre-dose (Each cycle is of 21 days)]
|
AUCinf is defined as area under the serum concentration versus time curve (AUC) from time zero (pre-dose) to extrapolated infinite time (0-inf).
|
Cycle 1: Pre-dose up to 336 hours post-dose; Cycle 2: 504 hours post-dose; Cycle 3: Pre-dose (Each cycle is of 21 days)]
|
Phase 1 and 2: Elimination Half-Life Time (T1/2) of EU101
Time Frame: Cycle 1: Pre-dose up to 336 hours post-dose; Cycle 2: 504 hours post-dose; Cycle 3: Pre-dose (Each cycle is of 21 days)]
|
T1/2 is defined as plasma decay half-life is the time measured for the serum concentration to decrease by one half.
|
Cycle 1: Pre-dose up to 336 hours post-dose; Cycle 2: 504 hours post-dose; Cycle 3: Pre-dose (Each cycle is of 21 days)]
|
Phase 1 and 2: Apparent Volume of Distribution (Vd/F) of EU101
Time Frame: Baseline (Day 1)
|
Vd/F is defined as volume of distribution is defined as the theoretical volume in which the total amount of drug would need to be uniformly distributed to produce the desired serum concentration of a drug.
|
Baseline (Day 1)
|
Phase 1 and 2: Apparent Oral Clearance of (CL/F) of EU101
Time Frame: Baseline (Day 1)
|
Clearance of a drug is a measure of the rate at which a drug is metabolized or eliminated by normal biological processes.
|
Baseline (Day 1)
|
Phase 1 and 2: Mean Residence Time (MRT) of EU101
Time Frame: Baseline (Day 1)
|
MRT is defined as AUMC(0 - inf) divided by AUC(0 - inf), where AUMC(0 - inf) is the area under the first moment curve from time 0 extrapolated to infinite time.
|
Baseline (Day 1)
|
Phase 1 and 2: Renal clearance (CLr) of EU101
Time Frame: Baseline (Day 1)
|
CLr is defined as renal clearance is the volume of plasma completely cleared of EU101 by the kidneys per unit time.
|
Baseline (Day 1)
|
Phase 1 and 2: Number of Participants with Positive Antidrug Antibodies (ADA)
Time Frame: Baseline up to 56 months
|
The immunogenic potential of EU101 will be assessed by summarizing the number of participants who develop detectable antidrug antibody (ADAs).
|
Baseline up to 56 months
|
Phase 2: Number of Participants With AEs and SAEs by Common Terminology Criteria for Adverse Events (CTCAE) v5.0
Time Frame: Time from first dose of study treatment up to 30 months
|
Time from first dose of study treatment up to 30 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 31, 2021
Primary Completion (Estimated)
September 1, 2025
Study Completion (Estimated)
December 1, 2025
Study Registration Dates
First Submitted
May 17, 2021
First Submitted That Met QC Criteria
May 25, 2021
First Posted (Actual)
May 27, 2021
Study Record Updates
Last Update Posted (Actual)
March 15, 2024
Last Update Submitted That Met QC Criteria
March 13, 2024
Last Verified
March 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Neoplasms by Histologic Type
- Neoplasms
- Urologic Neoplasms
- Urogenital Neoplasms
- Neoplasms by Site
- Kidney Diseases
- Urologic Diseases
- Adenocarcinoma
- Carcinoma
- Neoplasms, Glandular and Epithelial
- Genital Neoplasms, Male
- Prostatic Diseases
- Kidney Neoplasms
- Female Urogenital Diseases
- Female Urogenital Diseases and Pregnancy Complications
- Urogenital Diseases
- Male Urogenital Diseases
- Genital Diseases, Male
- Genital Diseases
- Carcinoma, Renal Cell
- Prostatic Neoplasms
Other Study ID Numbers
- EU-CTS101-I-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Yes
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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