Capivasertib: 400 mg (2 oral tablets) given on an intermittent weekly dosing schedule. Dosed on Days 2 to 5 of Weeks 1, 2, and 3 followed by 1 week off-treatment within each 28-day treatment cycle. Study treatment will be continued until disease progression unless there is evidence of unacceptable toxicity, or if the patient requests to stop the study treatment.
Paclitaxel: 80 mg/m2 concentrate for solution for infusion, 3 consecutive weekly infusions of 80 mg/m2 (given on Day 1 of Weeks 1, 2, and 3), followed by 1 week off-treatment within each 28-day treatment cycle. Paclitaxel treatment will be continued for at least 6 cycles unless the patient experiences unacceptable toxicity that is attributed directly to treatment with paclitaxel.
Placebo: Placebo: Oral tablets. 400 mg of Placebo (2 tablets) BD given on an intermittent weekly dosing schedule. Dosed on Days 2 to 5 of Weeks 1, 2, and 3 followed by 1 week offtreatment within each 28-day treatment cycle
Study summary
Phase III Study of Capivasertib + Paclitaxel versus Placebo + Paclitaxel as First line Treatment for Patients with Locally Advanced or Metastatic Triple-negative Breast Cancer (TNBC)
Eligibility
Sex
ALL
Min age
18 Years
Max age
130 Years
Healthy volunteers
No
Inclusion Criteria:
1. Histologically confirmed TNBC from most recently collected tumour tissue sample
2. Metastatic or locally recurrent disease; locally recurrent disease most not be amenable to resection with curative intent (patient who are considered suitable for surgical or ablative techniques following potential down-staging with study treatment are not eligible)
3. ECOG/WHO PS: 0-1
4. Measurable disease according to RECIST 1.1 and/or lytics or mixedbone lesions that can be assessed by CT or MRI in the absence of measurable disease
5. FFPE tumour sample from primary/recurrent cancer
Exclusion Criteria:
1. Prior Chemotherapy in the neoadjuvant or adjuvant setting within 6 months from the end of chemotherapy to the date of randomization; taxane chemotherapy in the neoadjuvant or adjuvant setting within 12 months from the end of chemotherapy to the start of randomization
2. Prior systematic therapy for inoperable locally advanced or metastatic disease
3. Prior treatment with any of the treatments listed below. Patients are not eligible to enter the study if they have received any of the medications specified below or are unable to meet the cautions and restrictions:
* AKT, PI3K, and/or mTOR inhibitors
* Capivasertib in the present study (ie, any dosing with capivasertib due to previous participation in this study)
* Any other chemotherapy, immunotherapy, immunosuppressant medication (other than corticosteroids) or anticancer agents within 3 weeks of the first dose of study treatment. A longer washout may be required for drugs with a long halflife (eg, biologics) as agreed by the sponsor
* Potent inhibitors or inducers of CYP3A4 within 2 weeks prior to the first dose of study treatment (3 weeks for St John's wort), or drugs that are sensitive to CYP3A4 inhibition within 1 week prior to the first dose of study treatment.
4. Radiotherapy with a wide field of radiation within 4 weeks before the first dose of study treatment (capivasertib/placebo)
5. Pre-existing sensory or motor polyneuropathy ≥grade 2 according to NCI CTCAE v5
6. With the exception of alopecia, any unresolved toxicities from prior therapy greater than CTCAE grade 1 at the time of starting study treatment
7. Any of the following cardiac criteria at screening:
* Mean resting corrected QT interval (QTc) \>470 msec obtained from 3 consecutive ECGs
* Any clinically important abnormalities in rhythm, conduction or morphology of resting ECG (eg, complete left bundle branch block, third degree heart block)
* Any factors that increase the risk of QTc prolongation or risk of arrhythmic events such as heart failure, hypokalaemia, potential for Torsades de Pointes, congenital long QT syndrome, family history of long QT syndrome or unexplained sudden death under 40 years of age or any concomitant medication known to prolong the QT interval
* Experience of any of the following procedures or conditions in the preceding 6 months: coronary artery bypass graft, angioplasty, vascular stent, myocardial infarction, angina pectoris, congestive heart failure New York Heart Association (NYHA) grade ≥2
* Uncontrolled hypotension - SBP \<90 mmHg and/or DBP \<50 mmHg
* Cardiac ejection fraction outside institutional range of normal or \<50% (whichever is higher) as measured by echocardiogram (or multiplegated acquisition \[MUGA\] scan if an echocardiogram cannot be performed or is inconclusive).
8. Clinically significant abnormalities of glucose metabolism as defined by any of the following at screening:
* Patients with diabetes mellitus type I or diabetes mellitus type II requiring insulin treatment
* HbA1c ≥8.0% (63.9 mmol/mol)
9. Inadequate bone marrow reserve or organ function at screening
10. Currently pregnant (confirmed with positive pregnancy test) or breast-feeding
Primary outcome measure(s)
Overall Survival (OS) — The time from date of randomisation to the date of death due to any cause up to approximately 42 months Overall Survival (OS)
Trial sites (260)
Facility
City
Region
Status
Research Site
Whittier
California
Research Site
Whittier
California
Research Site
Fort Myers
Florida
Research Site
Miami
Florida
Research Site
St. Petersburg
Florida
Research Site
Tampa
Florida
Research Site
Chicago
Illinois
Research Site
Westwood
Kansas
Research Site
Silver Spring
Maryland
Research Site
Detroit
Michigan
Research Site
Nyack
New York
Research Site
Cincinnati
Ohio
Research Site
Columbus
Ohio
Research Site
Harrisburg
Pennsylvania
Research Site
Philadelphia
Pennsylvania
Research Site
Pittsburgh
Pennsylvania
Research Site
Nashville
Tennessee
Research Site
Austin
Texas
Research Site
Fort Worth
Texas
Research Site
Houston
Texas
Research Site
San Antonio
Texas
Research Site
Fairfax
Virginia
Research Site
Buenos Aires
Argentina
Research Site
CABA
Argentina
Research Site
CABA
Argentina
Research Site
CABA
Argentina
Research Site
CABA
Argentina
Research Site
Ciudad Autonomade Buenos Aires
Argentina
Research Site
La Plata
Argentina
Research Site
Mar del Plata
Argentina
Research Site
Rosario
Argentina
Research Site
Barretos
Brazil
Research Site
Florianópolis
Brazil
Research Site
Goiânia
Brazil
Research Site
Londrina
Brazil
Research Site
Natal
Brazil
Research Site
Porto Alegre
Brazil
Research Site
Porto Alegre
Brazil
Research Site
Rio de Janeiro
Brazil
Research Site
São José do Rio Preto
Brazil
+ 220 more sites — see the full list on the official registry below.
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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