[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"healthy-male-participants\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:healthy-male-participants":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,41],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":4},"100650166","phase-1-evaluate-the-effect-of-vimseltinib-on-p-glycoprotein-p-gp-inhibition-in-healthy-male-participants-100650166",false,"NCT07744802","Evaluate the Effect of Vimseltinib on P-glycoprotein (P-gp) Inhibition in Healthy Male Participants","A Phase 1, Open-label, Fixed-sequence Study to Evaluate the Effect of Vimseltinib on P-glycoprotein (P-gp) Inhibition in Healthy Male Participants","Inclusion Criteria:\n\n1. Participants are in good general health, as required by the protocol and as determined by Principal Investigator.\n2. Body mass index (BMI) from greater than or equal to (≥) 18 to less than or equal to ≤ 32 kilogram per square meter (kg\u002Fm\\^2).\n3. Adequate organ function and blood and urine tests, as required by the protocol and as determined by Principal Investigator.\n\nExclusion Criteria:\n\n1. History or presence of clinically significant diseases of the neurological, dermatological, renal, hepatic, gastrointestinal, cardiovascular, or musculoskeletal systems or history or presence of clinically significant psychiatric, immunological, endocrine, or metabolic disease as determined by Principal Investigator.\n2. Unwilling or unable to comply with the requirements of the protocol.\n3. Determined by Principal Investigator to be unsuitable to participate in the study for any other reason.",true,"MALE","18 Years","55 Years",{"count":21,"type":22},20,"ESTIMATED","INTERVENTIONAL",[25],"PHASE1","The main purpose of this study is to determine the effect of vimseltinib on pharmacokinetics of P-glycoprotein (P-gp) substrate (dabigatran) in healthy male participants. This study will last approximately 21 days.",[28],"Healthy Male Participants","NOT_YET_RECRUITING","2026-07-30",{"date":32,"type":33},"2026-08-04","ACTUAL",{"date":35,"type":22},"2026-08",{"date":37,"type":22},"2027-12",{"name":39,"class":40},"Deciphera Pharmaceuticals, LLC","INDUSTRY",{"id":42,"slug":43,"hasResults":11,"nctId":44,"briefTitle":45,"officialTitle":46,"acronym":4,"eligibilityCriteria":47,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":48,"enrollmentInfo":49,"targetDuration":4,"studyType":23,"phases":51,"briefSummary":52,"conditions":53,"keywords":4,"overallStatus":54,"whyStopped":4,"lastUpdateSubmitDate":55,"lastUpdatePostDateStruct":56,"startDateStruct":58,"completionDateStruct":60,"leadSponsor":62,"locationsCount":64},"100616003","phase-1-a-phase-1-comparative-study-to-evaluate-pharmacokinetics-immunogenicity-safety-and-tolerability-of-bmab3000-and-herceptin-hylecta-after-a-single-600-mg-sc-injection-in-healthy-male-volunteers-100616003","NCT07299955","A Phase 1 Comparative Study to Evaluate Pharmacokinetics, Immunogenicity, Safety and Tolerability of Bmab3000 and Herceptin Hylecta® After a Single 600 mg SC Injection in Healthy Male Volunteers","A Phase 1, Randomized, Double-Blind, Two-arm, Parallel Design, Comparative Study to Assess Pharmacokinetics, Immunogenicity, Safety and Tolerability of Bmab3000 and Herceptin Hylecta® Following a Single Dose of 600 mg Subcutaneous Injection in Healthy Male Volunteers","Inclusion Criteria:\n\n1. Healthy male volunteers aged between 18 to 65 years; both inclusive.\n2. Body weight ≥50 kg and ≤100 kg with body mass index (BMI) between 18.5 and 30 kg\u002Fm2, both inclusive.\n3. Participants should have Left ventricular ejection fraction (LVEF) ≥55%.\n4. Male participants must be using an acceptable method of contraception for the entire duration of the trial, and for at least three months after the trial drug administration. Participants must refrain from fathering a child or donating sperm in the next three months following the last trial drug administration or undergoing vasectomy.\n5. All non-prescription medications must have been discontinued at least 14 days prior to dosing.\n6. All non-topical prescription medications must have been stopped at least 30 days prior to admission to the clinical research center.\n7. Absence of significant findings in the vital signs, 12 lead ECG, and clinical laboratory tests of blood and urine.\n8. Willing and able to sign the informed consent form (ICF).\n\nExclusion Criteria:\n\n1. History of previous exposure to trastuzumab.\n2. Presence of clinically significant medical history and clinically significant findings in the physical examination.\n3. Allergy or hypersensitivity to trastuzumab, other recombinant human or humanized antibodies, other related products, or any excipients\u002F ingredients (e.g. hyaluronidase).\n4. Sick sinus syndrome or known long QT syndrome (QTcF \\>450 msec).\n5. Pronounced sinus bradycardia (\\\u003C40 bpm), even if elicited by sport.\n6. History of relevant drug and\u002For food allergies.\n7. Positive urine drug and breath alcohol screen.\n8. Consumption of any foods containing poppy seeds within 48 hours (2 days) prior to screening\u002Fadmission to the clinical research center.\n9. Positive screen for hepatitis B surface antigen (HBsAg), anti-hepatitis virus (HCV) antibodies, anti-human immunodeficiency virus (HIV) 1 and 2 antibodies.\n10. Donation or loss of blood prior to drug administration.","65 Years",{"count":50,"type":22},150,[25],"This phase I study is to compare the pharmacokinetics (PK), immunogenicity, safety, and tolerability of Bmab3000 (test) and Herceptin Hylecta (reference) after a single subcutaneous (s.c.) dose in healthy male volunteers.",[28],"RECRUITING","2026-04-02",{"date":57,"type":33},"2026-04-08",{"date":59,"type":33},"2026-02-28",{"date":61,"type":22},"2026-06-30",{"name":63,"class":40},"Biocon Biologics UK PLC",1]