NCT07726433 Fosrolapitant Combined With Palonosetron to Prevent Trastuzumab Rezetecan Related CINV
| NCT ID | NCT07726433 |
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Tianjin Medical University Cancer Institute and Hospital |
| Condition | Chemotherapy-Induced Nausea and Vomiting (CINV) |
| Study Type | INTERVENTIONAL |
| Enrollment | 56 participants |
| Start Date | 2026-06-15 |
| Primary Completion | 2028-06-01 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
In Phase 2, researchers evaluate early signs of effectiveness. You may be randomized to receive the active treatment or a comparator. Monitoring continues closely.
This trial targets 56 participants in total. It began in 2026-06-15 with a primary completion date of 2028-06-01.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
This study is a prospective, single-arm, multicenter, exploratory clinical trial divided into a screening phase, a treatment phase, and a follow-up phase. The study aims to evaluate the efficacy and safety of foslorapitant palonosetron for injection in preventing nausea and vomiting caused by treatment with recanituzumab. All patients who meet the inclusion criteria and do not meet any exclusion criteria are eligible for enrollment in this study and are scheduled to receive targeted therapy, antiemetic treatment, and follow-up. Dosage Regimen Eligible subjects will receive a prophylactic antiemetic regimen consisting of foslorapitant and palonosetron. The dosage regimen is as follows: Day 1 (D1): Foslorapitant and palonosetron (218 mg foslorapitant and 0.25 mg palonosetron hydrochloride), administered intravenously (IV) 1 hour prior to chemotherapy. Observe for two treatment cycles (C1-C2); Starting from the first dose, record the patient's daily vomiting frequency, severity of nausea, and medication adherence.
Eligibility Criteria
Inclusion Criteria: 1. Sign a written informed consent form and voluntarily enroll in this study; 2. Be at least 18 years of age; gender is not a restriction; 3. Be a patient scheduled to receive treatment with Trastuzumab Rezetecan; 4. Have an ECOG performance status score of 0-2; 5. No ascites or pleural effusion requiring drainage; 6. No gastrointestinal obstruction, such as pyloric stenosis or intestinal obstruction; 7. Expected survival of ≥12 weeks; 8. Good organ and bone marrow function, defined as follows: Hematologic System (No blood transfusions or treatment with hematopoietic growth factors within the past 14 days) * Absolute Neutrophil Count (ANC) ≥ 1.5×10⁹/L * Platelets (PLT) ≥ 100×10⁹/L * Hemoglobin (Hb) ≥ 90 g/L Liver Function * Total Bilirubin (TBIL) ≤ 1.5×ULN (For patients with Gilbert's syndrome: ≤ 3×ULN) * Alanine Aminotransferase (ALT) ≤ 2.5×ULN (Patients with liver metastases: ≤ 5×ULN) * Aspartate Aminotransferase (AST) ≤ 2.5×ULN (Patients with liver metastases: ≤ 5×ULN) * Albumin (ALB) ≥ 30 g/L Renal Function * Creatinine (Cr) ≤ 1.5×ULN * Creatinine Clearance (Ccr) * (Calculated only when creatinine \> 1.5×ULN) Endogenous creatinine clearance ≥ 50 mL/min (Cockcroft-Gault formula) Cardiac Function * 12-lead electrocardiogram No severe arrhythmias, and a mean Fridericia-corrected QT interval (QTc) of \<450 ms (males) or \<470 ms (females) * Echocardiogram Left ventricular ejection fraction (LVEF) ≥ 50% 9. Agree to cooperate in completing daily nausea and vomiting logs and scale assessments; 10. Understand the nature of this study; the patient and/or legal guardian voluntarily agree to participate in this trial and sign the informed consent form. Exclusion Criteria: 1. Allergy to the study drug or its excipients; 2. Known contraindications to NK-1 receptor antagonists, 5-HT3 receptor antagonists, or dexamethasone; 3. Nausea or vomiting at the time of enrollment requiring treatment with antiemetics; 4. Use of medications with antiemetic effects within 2 days prior to the first dose; 5. Initiation of potent opioid analgesics within 48 hours prior to enrollment (adjustment of the dose of medications already in use is permitted); 6. Presence of conditions affecting the assessment of vomiting, such as gastrointestinal obstruction, gastroparesis, or intestinal obstruction; 7. Patients who are difficult to enroll due to clinically diagnosed psychiatric disorders; 8. Localized or active systemic infections requiring treatment; 9. Pregnant or breastfeeding women, as well as patients of childbearing age who refuse to use appropriate contraceptive measures during the course of this trial; 10. Patients who have participated in other clinical trials within 30 days prior to the first dose of the study drug (patients who failed screening for other clinical trials may be enrolled in this study); 11. Patients with other factors deemed by the investigator to be unsuitable for participation in this study, such as any physiological or psychological conditions that may increase study risks, affect patient adherence to the protocol, or interfere with the patient's ability to complete the trial.
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07726433 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Chemotherapy-Induced Nausea and Vomiting (CINV). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
What phase is the NCT07726433 trial and what does that mean for participants?
Phase 2 trials evaluate whether the treatment shows signs of effectiveness while continuing to monitor safety. More participants are enrolled than in Phase 1 to help refine the treatment protocol.
Is NCT07726433 currently recruiting?
Yes, NCT07726433 is actively recruiting participants. Contact the research team at zhjiang@tmu.edu.cn for enrollment information.
Where is the NCT07726433 trial being conducted?
This trial is being conducted at Tianjin, China.
Who is sponsoring the NCT07726433 clinical trial?
NCT07726433 is sponsored by Tianjin Medical University Cancer Institute and Hospital. The trial plans to enroll 56 participants.