NCT06974604 Preventing Dato-DXd Associated Stomatitis With Dexamethasone Mouthwash, TROPION-DM
| NCT ID | NCT06974604 |
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Brown University |
| Condition | Breast Neoplasms |
| Study Type | INTERVENTIONAL |
| Enrollment | 60 participants |
| Start Date | 2025-10-22 |
| Primary Completion | 2027-05-31 |
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 60 participants in total. It began in 2025-10-22 with a primary completion date of 2027-05-31.
⚠ 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
TROPION-DM/BrUOG-431 is a prospective, , phase 2 trial with two non-comparative cohorts analyzed jointly for primary endpoint in adult patients with either (Cohort 1:) advanced/metastatic hormone-receptor positive (\[HR+\], estrogen receptor and/or progesterone receptor positive) breast cancer (BC), or advanced/metastatic triple negative breast cancer (TNBC) or (Cohort 2:) advanced/metastatic non-squamous non-small cell lung cancer (NSCLC). All patients will be treated with Datopotumab deruxtecan (Dato-DXd) at 6 mg/kg IV every 3 weeks until disease progression or unacceptable toxicity. Due to the risk of stomatitis, the investigational component of this trial will be to incorporate alcohol-free dexamethasone mouthwash, 10 mL 0.5 mg/5mL oral solution, days 1-5, swish and spit four times daily for the first 3 cycles.
Eligibility Criteria
Inclusion Criteria: * Has advanced and/or metastatic cancer that meets one of the following criteria: 1. Pathologically documented unresectable advanced non-squamous NSCLC not amenable to curative therapy that has progressed on at least one prior therapy. 2. Pathologically documented triple negative breast cancer (estrogen receptor negative and progesterone receptor negative and HER2 negative) who have progressed on at least 1 prior line of therapy or in the opinion of the treating physician, not be a candidate for standard first-line metastatic breast cancer therapy 3. Pathologically documented hormone receptor positive breast cancer (estrogen receptor and/or progesterone receptor positive, HER2 negative) which has progressed on hormonal based therapy including CDK4/6 inhibitor and 1 prior line of chemotherapy and/or antibody drug conjugate therapy. * Aged ≥18 years. * Has an Eastern Cooperative Oncology Group performance status 0-2. * Has a left ventricular ejection fraction (LVEF) 50% by either an echocardiogram (ECHO) or multiple gated acquisition scan (MUGA) within 28 days before enrollment. * Measurable disease based on Response Evaluation Criteria in Solids Tumors (RECIST) version 1.1. * Has adequate organ function that would make them an appropriate candidate for Datopotamab deruxtecan therapy as treatment of advanced metastatic cancer as assessed by the treating physician, which shall include results of complete blood count with differential, and comprehensive metabolic panel within 14 days before Cycle 1, Day 1, defined as: 1. Platelet count ≥100,000/mm3 2. Hemoglobin ≥9.0 g/dL 3. Absolute neutrophil count ≥1000/mm3 4. Creatinine clearance ≥30 mL/min as calculated using the Cockcroft-Gault equation. 5. Aspartate aminotransferase ≤3 ×ULN (if liver metastases are present, ≤5 × ULN) 6. Alanine aminotransferase ≤3 × ULN (if liver metastases are present, ≤5 × ULN) 7. Total bilirubin ≤1.5 × ULN if no liver metastases or liver \< 3 if liver metastases are present. * Has an adequate treatment washout period prior to Cycle 1, Day 1, defined as appropriately recovering from: 1. Major surgery: ≥2 weeks (or 2 weeks for low-invasive cases \[eg, colostomy\]). 2. Radiation therapy (curative) and palliative radiation therapy to lung fields: ≥4 weeks; ≥2 weeks (palliative radiation therapy to other areas \[ie, limited field and 10 or fewer days or fractions\] including whole brain radiotherapy). 3. Hormonal therapy: ≥2 weeks 4. Chemotherapy (including immunotherapy \[non-antibody based therapy\]), and retinoid therapy: ≥2 weeks or 5 times terminal elimination half-life (T½) of the chemotherapeutic agent (whichever is longer); ≥6 weeks for nitrosoureas or mitomycin C, ≥1 week for tyrosine kinase inhibitors (TKIs) 5. Antibody-based anti-cancer therapy: ≥4 weeks 6. Chloroquine/hydroxychloroquine: \>14 days * If of reproductive/child-bearing potential, agrees to use a highly effective form of contraception or avoid intercourse throughout treatment and upon completion of the study for at least 7 months for females and 4 months for males after the last dose of study drug. Highly effective methods of birth control include: combined (estrogen and progesterone containing) hormonal contraception by oral or intravaginal route or dermal patches; progesterone-only hormonal contraception associated with inhibition of ovulation given by oral route or by injections or implants; intrauterine device (IUD); intrauterine hormone-releasing system (IUS); bilateral tubal occlusion; vasectomized partner (with confirmation of surgical success); and complete heterosexual abstinence. * Starting at the time of randomization/first dose of study intervention male subjects/participants must not freeze or donate sperm at any time during this study and for at least 4 months after the last dose of Dato-DXd. Preservation of sperm should be considered prior to randomization/first dose of study intervention. * Starting at the time of randomization/first dose of study intervention female subjects/participants must not breastfeed or donate, or retrieve for their own use, ova at any time during this study and for at least 7 months after the last dose of Dato-DXd. Preservation of ova should be considered prior to randomization/first dose of study intervention. * Is able to provide written informed consent and is willing and able to comply with the protocol. Subject must be fully informed about their illness and the investigational nature of the study protocol (including foreseeable risks and possible toxicities) and must sign and date the Institutional Review Board (IRB)/Independent ethics committee (IEC) approved informed consent form (ICF) (including Health Insurance Portability and Accountability Act authorization \[HIPAA\], if applicable) before performance of any study- specific procedures or examinations. * Willingness to self-report level of oral pain using Visual Analog Scale (VAS) and the Normalcy Diet Scale (NDS) throughout each stomatitis event. (40, 41) At baseline, patient's self-reported oral pain level, using VAS, must be 0 (See Appendix B) and the normalcy diet scale score should ≥ 60 (See Appendix C). * Willingness to record oral symptoms in Oral Diary (See Appendix D). * Has a life expectancy of ≥3 months. Exclusion Criteria: * Active second malignancy which would alter interpretation of study results. * Has a history of non-infectious ILD/pneumonitis including radiation pneumonitis that required steroids, has current ILD/pneumonitis, or where suspected ILD/pneumonitis cannot be ruled out by imaging at screening. * Has clinically significant corneal disease * Has a history of severe hypersensitivity reactions to either the drug or inactive ingredients (including but not limited to polysorbate 80) of Dato-DXd. * Has a history of severe hypersensitivity reactions to other monoclonal antibodies. * Has ongoing radiation-related toxicities * Has an uncontrolled infection requiring intravenous (IV) antibiotics, antivirals, or antifungals. * Has active human immunodeficiency virus (HIV) infection that is not well controlled. * Has an active or uncontrolled hepatitis B and/or hepatitis C infection * Is lactating or pregnant as confirmed by pregnancy tests performed within 7 days before enrollment. * Clinically severe pulmonary compromise resulting from autoimmune, connective tissue or inflammatory disorders with pulmonary involvement. * Has uncontrolled or significant cardiac disease (including MI or unstable angina within the past 6 months, NYHA Class II-IV heart failure, uncontrolled hypertension, uncontrolled or significant arrhythmia). Patients with the following may be enrolled based on the investigator's/treating physician's assessment (documentation must be submitted to BrUOG). -Mean resting corrected QTcF interval \> 470 ms. * History of QT prolongation associated with other medications that required discontinuation of that medication, or any current concomitant medication known to prolong the QT interval and cause Torsades de Pointes. * Congenital long QT syndrome, family history of long QT syndrome, or unexplained sudden death under 40 years of age in first-degree relatives.
Contact & Investigator
Stephanie Graff, MD
PRINCIPAL INVESTIGATOR
Rhode Island and the Miriam Hospitals (Brown University Health)
Frequently Asked Questions
Who can join the NCT06974604 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Breast Neoplasms. 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 NCT06974604 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 NCT06974604 currently recruiting?
Yes, NCT06974604 is actively recruiting participants. Contact the research team at BrUOG@brown.edu for enrollment information.
Where is the NCT06974604 trial being conducted?
This trial is being conducted at Providence, United States.
Who is sponsoring the NCT06974604 clinical trial?
NCT06974604 is sponsored by Brown University. The principal investigator is Stephanie Graff, MD at Rhode Island and the Miriam Hospitals (Brown University Health). The trial plans to enroll 60 participants.