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giredestrant

Generic: Giredestrant

giredestrant: 7 clinical trials tracked.

giredestrant evidence translation

What we can confirm

7 tracked trials

No verified listed developer

What it means

AI will separate confirmed drug evidence from unknown company context.

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Watch trial status, endpoints, and the next source-backed update.
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Prepared research question

What is verified about giredestrant, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence4 indications · 2 study sponsors
Clinical Trials (7)

A Phase III Randomized, Open-Label Study Evaluating Efficacy and Safety of Giredestrant Compared With Fulvestrant, Both Combined With a CDK4/6 Inhibitor, in Patients With Estrogen Receptor-Positive, HER2-Negative Advanced Breast Cancer With Resistance to Prior Adjuvant Endocrine Therapy

NCT06065748·Phase 3·ENTA
Recruiting

Primary endpoint: Progression-Free Survival (PFS) in the ESR1 mutation (ESR1m) Subgroup

InterventionalRandomizedopen1,050 targetStarted 2023-12Completion 2029-0250 sites · United StatesHoffmann-La Roche

A Phase IB/II Multi-Cohort Study of Targeted Agents and/or Immunotherapy With Atezolizumab for Patients With Recurrent or Persistent Endometrial Cancer

NCT04486352·Phase 1/Phase 2
Recruiting

Primary endpoint: Investigator-assessed overall response rate (ORR) of each biomarker cohort

Interventionalopen148 targetStarted 2021-10Completion 2027-1021 sites · United StatesAlliance Foundation Trials, LLC.

A Phase III, Randomized, Open-Label, Multicenter Study Evaluating the Efficacy and Safety of Adjuvant Giredestrant Compared With Physician's Choice of Adjuvant Endocrine Monotherapy in Patients With Estrogen Receptor-Positive, HER2-Negative Early Breast Cancer

NCT04961996·Phase 3·ENTA
Active, not recruiting

Primary endpoint: Invasive Disease-Free Survival (IDFS), Excluding Second Primary Non-Breast Cancers

InterventionalRandomizedopen4,170 targetStarted 2021-08Completion 2035-0150 sites · United StatesHoffmann-La Roche

A Phase Ib/II, Open-Label, Multicenter, Randomized Umbrella Study Evaluating the Efficacy and Safety of Multiple Treatment Combinations in Patients With Breast Cancer (MORPHEUS-BREAST CANCER)

NCT04802759·Phase 1·ENTA
Recruiting

Primary endpoint: Percentage of Participants with Objective Response, Defined as a Complete or Partial Response, as Determined by the Investigator According to Response Evaluation Criteria in Solid Tumors, version 1.1 (RECIST v1.1)

InterventionalRandomizedopen316 targetStarted 2021-06Completion 2029-0531 sites · Australia, Israel, South Korea, Spain…Hoffmann-La Roche

A Phase III Randomized, Double-Blind, Placebo-Controlled, Multicenter Study Evaluating the Efficacy and Safety of GDC-9545 Combined With Palbociclib Compared With Letrozole Combined With Palbociclib in Patients With Estrogen Receptor-Positive, HER2-Negative Locally Advanced or Metastatic Breast Cancer

NCT04546009·Phase 3·ENTA
Active, not recruiting

Primary endpoint: Progression-Free Survival (PFS), as Determined by the Investigator According to RECIST v1.1

InterventionalRandomizeddouble992 targetStarted 2020-10Completion 2028-0350 sites · Argentina, Australia, United StatesHoffmann-La Roche

A Phase Ib/II, Open-label, Multicenter, Randomized Umbrella Study Evaluating the Efficacy and Safety of Multiple Treatment Combinations in Patients With Metastatic Breast Cancer (Morpheus-panBC)

NCT03424005·Phase 1/Phase 2
Recruiting

Primary endpoint: Objective Response Rate (ORR)

InterventionalRandomizedopen1,132 targetStarted 2018-03Completion 2030-0949 sites · Australia, France, Germany, Israel…Hoffmann-La Roche

A Phase Ia/Ib, Multicenter, Open-Label, Dose Escalation, Dose Expansion Study Evaluating the Safety, Pharmacokinetics, and Activity of GDC-9545 Alone or in Combination With Palbociclib and/or LHRH Agonist in Patients With Locally Advanced or Metastatic Estrogen Receptor-Positive Breast Cancer

NCT03332797·Phase 1·MYOV
Active, not recruiting

Primary endpoint: Number of Participants with Adverse Events by Severity, According to National Cancer Institute Common Terminology Criteria for Adverse Events version 4.0 (NCI-CTCAE v4.0)

Interventionalopen181 targetStarted 2017-11Completion 2026-0723 sites · Australia, South Korea, Spain, United Kingdom…Genentech, Inc.