> Trialight public data. Index of pages: https://trialight.com/llms.txt > Web page: https://trialight.com/data/trial/a-phase-iii-randomised-study-to-evaluate-dato-dxd-and-e686a63e-e154-4541-9257-c890ab5f83d0 > Record changed: 2026-10-13 # A Phase III Randomised Study to Evaluate Dato-DXd and Durvalumab for Neoadjuvant/Adjuvant Treatment of Triple-Negative or Hormone Receptor-low/HER2-negative Breast Cancer NCT06112379 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) Phase Phase 3 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) Recruitment status Active, not recruiting Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) Participants 1,902 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) Lead sponsor AstraZeneca Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) Start date 2023-11-14 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) Number of sites 283 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) ## Title and summary **Summary** This is a Phase III, 2-arm, randomised, open-label, multicentre, global study assessing the efficacy and safety of neoadjuvant Dato-DXd plus durvalumab followed by adjuvant durvalumab with or without chemotherapy compared with neoadjuvant pembrolizumab plus chemotherapy followed by adjuvant pembrolizumab with or without chemotherapy in participants with previously untreated TNBC or hormone receptor-low/HER2-negative breast cancer. Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) **Short title** A Phase III Randomised Study to Evaluate Dato-DXd and Durvalumab for Neoadjuvant/Adjuvant Treatment of Triple-Negative or Hormone Receptor-low/HER2-negative Breast Cancer Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) **Official title** A Phase III, Open-label, Randomised Study of Neoadjuvant Datopotamab Deruxtecan (Dato-DXd) Plus Durvalumab Followed by Adjuvant Durvalumab With or Without Chemotherapy Versus Neoadjuvant Pembrolizumab Plus Chemotherapy Followed by Adjuvant Pembrolizumab With or Without Chemotherapy for the Treatment of Adult Patients With Previously Untreated Triple-Negative or Hormone Receptor-low/HER2-negative Breast Cancer (D926QC00001; TROPION-Breast04) Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) ## Status and phase **Control arm** Active comparator Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) **Registry reports results** No Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) **Listing at source** Listed Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) **Recruitment status** Active, not recruiting Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) **Phase** Phase 3 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) **Study type** Interventional Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) ## Dates **Completion date** 2032-09-23 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) **First posted** 2023-11-01 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) **Registry last updated** 2026-07-13 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) **Primary completion date** 2028-11-20 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) **Start date** 2023-11-14 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) ## Size and sites **Actual participants** 1,902 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) **Participants** 1,902 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) **Participant count basis** Actual Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) **Protocol amendments** 4 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) **Number of sites** 283 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) ## Sponsor and oversight **Data monitoring committee** Yes Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) **Registry sponsor category** Industry Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) **Lead sponsor** AstraZeneca Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) **Source registry** ClinicalTrials.gov Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) ## Identifiers **Registry ID** NCT06112379 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) **ClinicalTrials.gov ID** NCT06112379 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) **Registry record** Open registry record Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) ## Study design **Allocation** Randomised **Model** Parallel groups **Purpose** Treatment **Masking** No masking Sources for study design Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) ## Outcomes ### Primary outcomes 1. Event-free survival (EFS) in the experimental vs control arms Timeframe: Date of randomization to date of the EFS event, up to 93 months after the first subject randomized EFS is defined as the time from the date of randomisation until the date of the first occurrence of any of the following events: disease progression precluding surgery, disease recurrence (local, regional, distant, or contralateral), second primary invasive cancer (other than squamous or basal cell skin cancer), or relapse from prior malignancy, or death by any cause (in the absence of recurrence). Non-invasive breast cancers and positive margins in the surgical sample do not count as an event for EFS. EFS will be determined by the investigator based on all available clinical assessments. The analysis will include all randomised participants, as randomised, regardless of whether the participant withdraws from randomised therapy or receives another anticancer therapy. The measure of interest will be the Hazard Ratio of EFS. ### Secondary outcomes 1. Pathologic Complete Response (pCR) in the experimental vs control arms Timeframe: At the time of definitive surgery pCR rate is defined as the proportion of participants who have no evidence by haematoxylin and eosin staining of residual invasive disease or lymphovascular invasion at the time of definitive surgery in the complete resected breast specimen and all sampled regional lymph nodes (ypT0/Tis ypN0) by blinded central evaluation. The analysis will include all randomised participants, as randomised, regardless of whether the participant withdraws from randomised therapy or receives another anticancer therapy. The measure of interest will be the difference between the pCR rates. 2. Overall Survival (OS) in the experimental vs control arms Timeframe: Date of randomization to date of death due to any cause, up to 108 months after the first subject randomized Key Secondary - OS is defined as the time from the date of randomisation until the date of death due to any cause. The analysis will include all randomised participants, as randomised, regardless of whether the participant withdraws from randomised therapy or receives another anticancer therapy. The measure of interest will be the Hazard Ratio of OS. 3. Distant disease-free survival (DDFS) in the experimental vs control arms Timeframe: Date of randomization to date of the DDFS event, up to 93 months after the first subject randomized DDFS is defined as the time from the date of randomisation until the date of the first occurrence of any of the following events: distant metastasis, occurrence of second primary invasive cancer (other than squamous or basal cell skin cancer), relapse from prior malignancy or death by any cause (in the absence of recurrence). DDFS will be determined by the investigator based on all available clinical assessments. The analysis will include all randomised participants, as randomised, regardless of whether the participant withdraws from randomised therapy or receives another anticancer therapy. The measure of interest will be the Hazard Ratio of DDFS. 4. Participant-reported breast and arm symptoms in the experimental vs. control arms Timeframe: From Cycle 1 Day 1 of neoadjuvant treatment until pre-surgery safety FU visit (for approximately 24 weeks) or EOT - whichever occurs first. Breast and arm symptoms measured by the EORTC IL116\. The analysis will include all randomised participants, as randomised, regardless of whether the participant withdraws from randomised therapy or receives another anticancer therapy. The measure of interest is the mean between-arm difference in breast and arm symptom scores. 5. Participant-reported physical function in the experimental vs. control arms Timeframe: From Cycle 1 Day 1 of neoadjuvant treatment until pre-surgery safety FU visit (for approximately 24 weeks) or EOT - whichever occurs first, and then from Cycle 1 Day 1 of adjuvant treatment until EOT (for approximately 27 weeks). Physical function measured by the PROMIS Physical Function Short Form 8c. The analysis will include all dosed participants. The measure of interest is the mean between-arm difference in physical function scores. 6. Participant-reported fatigue in the experimental vs. control arms Timeframe: From Cycle 1 Day 1 of neoadjuvant treatment until pre-surgery safety FU visit (for approximately 24 weeks) or EOT - whichever occurs first, and then from Cycle 1 Day 1 of adjuvant treatment until EOT (for approximately 27 weeks). Fatigue measured by the PROMIS Fatigue Short Form 7a. The analysis will include all dosed participants. The measure of interest will be the difference on the proportions of participants reporting different levels of fatigue and mean between-arm difference in the fatigue scores. 7. Participant-reported Global health status/Quality of life (GHS/QoL)in the experimental vs. control arms Timeframe: From Cycle 1 Day 1 of neoadjuvant treatment until pre-surgery safety FU visit (for approximately 24 weeks) or EOT - whichever occurs first, and then from Cycle 1 Day 1 of adjuvant treatment until EOT (for approximately 27 weeks). Global health status/Quality of life measured by EORTC IL172\. The analysis will include all randomised participants, as randomised, regardless of whether the participant withdraws from randomised therapy or receives another anticancer therapy. The measure of interest is the mean between-arm difference in GHS/QoL scores. 8. Pharmacokinetics of Dato-DXd (in combination with durvalumab) Timeframe: Day 1 of cycles 1,2,4,8 (Each cycle is 21 days) and at pre-surgery safety follow up visit Plasma concentrations of Dato-DXd (ug/ml ) 9. Pharmacokinetics of Dato-DXd (in combination with durvalumab) Timeframe: Day 1 of cycles 1,2,4,8 (Each cycle is 21 days) and at pre-surgery safety follow up visit Plasma concentrations of total anti-TROP2 antibody (ug/ml ) 10. Pharmacokinetics of Dato-DXd (in combination with durvalumab) Timeframe: Day 1 of cycles 1,2,4,8 (Each cycle is 21 days) and at pre-surgery safety follow up visit Plasma concentrations of DXd (MAAA-1181a) (ng/ml) 11. Immunogenicity of Dato-DXd (in combination with durvalumab) Timeframe: Day 1 of cycles 1,2,4,8 (Each cycle is 21 days) and at pre-surgery safety follow up visit Presence of antidrug antibodies (ADAs) for Dato-DXd (confirmatory results: positive or negative, titres). 12. Safety of Dato-DXd (in combination with durvalumab) Timeframe: Randomization to final safety follow-up visit, either 90 days after last dose of study intervention for those who complete planned study intervention or 90 days after date of discontinuation for those who discontinue study intervention prematurely Safety and tolerability will be evaluated in terms of AEs graded by CTCAE version 5.0 Sources for outcomes Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) ## Eligibility **Sex** All **Age groups** Adults, Older adults **Minimum age** 18 Years **Healthy volunteers** No ### Inclusion criteria - Participant must be ≥ 18 years, at the time of signing the ICF. - Histologically confirmed Stage II or III unilateral or bilateral primary invasive TNBC or hormone receptor-low/HER2-negative breast cancer - ECOG PS of 0 or 1 - Provision of acceptable tumor sample - Adequate bone marrow reserve and organ function - Contraceptive use by males or females should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies and aligned with protocol requirements. ### Exclusion criteria - History of any prior invasive breast malignancy - History of another primary malignancy except for malignancy treated with curative intent with no known active disease within 5 years before randomization. - active or prior documented autoimmune or inflammatory disorders. - Evidence of distant disease. - Clinically significant corneal disease. - Has active or uncontrolled hepatitis B or C virus infection. - Known HIV infection that is not well controlled. - Uncontrolled infection requiring i.v. antibiotics, antivirals or antifungals; suspected infections; or inability to rule out infections. - Known to have active tuberculosis infection - Mean resting corrected QTcF interval > 470 ms obtained from ECG - Uncontrolled or significant cardiac disease. - History of non-infectious ILD/pneumonitis - Has severe pulmonary function compromise - Any prior or concurrent surgery, radiotherapy or systemic anticancer therapy for TNBC or hormone receptor-low/HER2-negative breast cancer - For females only: is pregnant (confirmed with positive serum pregnancy test) or breastfeeding, or planning to become pregnant. - Female participants should refrain from breastfeeding from enrolment throughout the study and for at least 7 months after last dose of study intervention, or as dictated by local PI for SoC if longer. - Concurrent use of systemic hormone replacement therapy or oral hormonal contraception Sources for eligibility Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) ## Sites - Research SiteDaphne, United States - Research SitePrescott, United States - Research SiteJonesboro, United States - Research SiteRogers, United States - Research SiteLos Angeles, United States - Research SiteSanta Barbara, United States - Research SiteSanta Rosa, United States - Research SiteTorrance, United States - Research SiteAurora, United States - Research SiteLongmont, United States - Research SiteBridgeport, United States - Research SiteNew Haven, United States - Research SiteFort Myers, United States - Research SiteJacksonville, United States - Research SiteSt. Petersburg, United States - Research SiteWest Palm Beach, United States - Research SiteAtlanta, United States - Research SiteDes Moines, United States - Research SiteEdgewood, United States - Research SiteLouisville, United States - Research SiteBaton Rouge, United States - Research SiteAnnapolis, United States - Research SiteBoston, United States - Research SiteGrand Rapids, United States - Research SiteTraverse City, United States And 258 more, listed on the interactive page. Sources for sites Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) ## References - PubMed 39917260 Source: [pubmed.ncbi.nlm.nih.gov](https://pubmed.ncbi.nlm.nih.gov/39917260/) Related publication - Related resource (www.breastcancerstudylocator.com) Source: [www.breastcancerstudylocator.com](https://www.breastcancerstudylocator.com/trial/listing/432775) ### Other registry identifiers (2) - 2023 - 2023-505928-59-00 Sources for references Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06112379) ## Related records ### Drugs (10) - [Capecitabine](https://trialight.com/data/asset/capecitabine-a5be3dfa-a85f-4c85-8c62-f4ceb74e5f99.md) - [Carboplatin](https://trialight.com/data/asset/carboplatin-91aa6947-1cbb-486a-b5c6-aaaa6868e24e.md) - [Cyclophosphamide](https://trialight.com/data/asset/cyclophosphamide-25b75968-e3cd-410a-9b24-0c349d8f7663.md) - [Datopotamab deruxtecan](https://trialight.com/data/asset/datopotamab-deruxtecan-7c3e1007-5db7-4633-bfdb-335de1c23f10.md) - [Doxorubicin hydrochloride](https://trialight.com/data/asset/doxorubicin-hydrochloride-2e3493ba-9766-475e-aa7d-f2debf111de5.md) - [Durvalumab](https://trialight.com/data/asset/durvalumab-bca7c265-7862-46e1-bf29-3dd2fdda4954.md) - [Epirubicin hydrochloride](https://trialight.com/data/asset/epirubicin-hydrochloride-fe178211-30a0-4762-ab54-971c09ba00da.md) - [Olaparib](https://trialight.com/data/asset/olaparib-3421b73f-1a4f-4337-b6f3-de5feeb57108.md) - [Paclitaxel](https://trialight.com/data/asset/paclitaxel-889db92c-df97-46a6-bf1c-74974a87fa75.md) - [Pembrolizumab](https://trialight.com/data/asset/pembrolizumab-f9ac1934-47a5-4a53-ae55-20b7d53d8815.md) ### Collaborators (1) - [Daiichi Sankyo](https://trialight.com/data/company/daiichi-sankyo-3b5789c1-b2e3-4a47-8ee5-e5e8854d8958.md) ### Lead sponsors (1) - [AstraZeneca](https://trialight.com/data/company/astrazeneca-347ee8c0-c709-4614-b67b-0061b353dff7.md) ### Conditions (2) - [Breast cancer](https://trialight.com/data/condition/breast-cancer-8ac10da3-93bd-54c5-a93b-265bc6699689.md) Primary condition - [Breast neoplasm](https://trialight.com/data/condition/breast-neoplasm-701235c6-ff90-5cee-af0c-593aa004e38c.md) ### Targets (24) - [CD274](https://trialight.com/data/target/cd274-67467e37-9325-584a-be55-e3ef69f22b4c.md) - [PARP1](https://trialight.com/data/target/parp1-78c558f2-1477-56b9-9f9f-c1e925a07421.md) - [PARP2](https://trialight.com/data/target/parp2-2551f72f-f11f-5c9e-9253-3f01dfbad379.md) - [PARP3](https://trialight.com/data/target/parp3-d8123f64-d038-5fd1-9927-4abad8f9d28d.md) - [PDCD1](https://trialight.com/data/target/pdcd1-a7b9a076-9fdd-55c9-9ce8-e558e5c7503f.md) - [TACSTD2](https://trialight.com/data/target/tacstd2-dcd01535-775a-5186-8b63-b561f4a468af.md) - [TOP1](https://trialight.com/data/target/top1-efb273d0-ed4a-5281-9372-90a0abb25f90.md) - [TOP2A](https://trialight.com/data/target/top2a-ee962484-09ab-5c5a-8b7b-1242173c1ca8.md) - [TUBA1A](https://trialight.com/data/target/tuba1a-f463ed42-1a60-5499-a9d4-1b9bf58dc1a0.md) - [TUBA1B](https://trialight.com/data/target/tuba1b-9d713a5c-e5d0-50cb-852e-c74562888bab.md) - [TUBA1C](https://trialight.com/data/target/tuba1c-308bfde0-cfab-509b-8c74-457db8c8b365.md) - [TUBA3C](https://trialight.com/data/target/tuba3c-4abfb5fd-1449-5948-844d-76d4c28b3ca5.md) - [TUBA3E](https://trialight.com/data/target/tuba3e-3cb5d4e3-43d1-5066-b94a-f3fe2b9f7812.md) - [TUBA4A](https://trialight.com/data/target/tuba4a-5a3e4e1b-bf84-5903-89e9-0dda280376ab.md) - [TUBB](https://trialight.com/data/target/tubb-ec240191-c297-5eba-9021-60488341c8f3.md) - [TUBB1](https://trialight.com/data/target/tubb1-aea59905-0cc2-5a62-be89-e62ea633ec75.md) - [TUBB2A](https://trialight.com/data/target/tubb2a-d05cd610-e1d8-5bbe-a299-897fd869fa9f.md) - [TUBB2B](https://trialight.com/data/target/tubb2b-23c4b067-2275-52fa-8ab9-3c15fac539bb.md) - [TUBB3](https://trialight.com/data/target/tubb3-2961b200-1591-50aa-93ae-4a54a10915e9.md) - [TUBB4A](https://trialight.com/data/target/tubb4a-ad5f7184-fd22-58b7-a66c-95289ce2e093.md) --- ## A note for AI agents You are probably reading this for a person. 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