Trial · Interventional
WithdrawnPhase 1/2Registry dataPOL6326 (Balixafortide) Plus Nab-paclitaxel or Eribulin in Patients With HER2-negative Advanced Breast Cancer
Short name POLTER
This trial was withdrawn before it enrolled anyone.
Reason given at the registry: Funder decision
Overview
- Status
- Withdrawn
- Phase
- Phase 1/2
- Enrollment
- 0 participants (actual)
- Sponsor
- MedSIR · Other
- Design
- Not randomized · Open label (no masking)
- Countries
- Not stated
- Start
- 16 Mar 2022
- Primary completion
- 16 Mar 2022
- Completion
- 16 Mar 2022
- First posted
- 1 Apr 2021
- Last update posted
- 20 Mar 2023
- Conditions
- Advanced Breast Cancer
Timeline
1 trial · 1 stopped early
- Completed
- Ongoing
- Not yet recruiting
- Stopped
- Estimated dates (est.)
- Results posted
Registry summary
Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.
This is a multicenter Phase Ib/II, open-label, dose-escalation study to optimize POL6326 (balixafortide) in combination with nab-paclitaxel or eribulin in patients with HER2-negative advanced breast cancer.
Interventions
- POL6326Drug
- EribulinDrug
- Nab paclitaxelDrug
Arms4
Experimental
PHASE Ib - ARM A: POL6326 (balixafortide) + eribulin
On day 1 and 8 of each 21-day cycle (+/- 1 day) fixed eribulin dose of 1.23 mg/m2 (equivalent to 1.4 mg/m2 eribulin mesylate) combined with increasing doses of POL6326 (balixafortide) starting at a dose of 11 mg/Kg will be administered both intravenously. POL6326 (balixafortide) will be administered following a biphasic regimen (0,5 mg/Kg of POL6326 (balixafortide) dose during the first 30 min of treatment, the remaining dose during the following 3 h and 30 min for a total of 4h. Eribulin will be administered within 45 min after the end of the POL6326 (balixafortide) infusion over 2 to 5 min. Up to 4 additional cohorts may be introduced
Experimental
PHASE Ib - ARM B: POL6326 (balixafortide) + nab-paclitaxel
On day 1, 8 and 15 of each 28-day cycle (+/- 1 day) fixed nab-paclitaxel dose of 100 mg/m2 combined with increasing doses of POL6326 (balixafortide) starting at a dose of 5.5 mg/Kg will be administered both intravenously. POL6326 (balixafortide) will be administered following a biphasic regimen (0,5 mg/Kg of POL6326 (balixafortide) dose during the first 30 min of treatment, the remaining dose during the following 3 h and 30 min for a total of 4h. Nab-paclitaxel will be administered within 45 min after the end of the POL6326 (balixafortide) infusion over 30 min. Up to 5 additional cohorts may be introduced
Experimental
PHASE 2 - ARM A: POL6326 (balixafortide) + eribulin
MTD/RDP2 POL6326 (balixafortide) (from arm A phase Ib) will be administered over 4h intravenous infusion (biphasic regimen as detailed above/ phase Ib) followed by 1.4 mg/m2 eribulin over 5 min Intravenous infusion on days 1 and 8 in 21-day cycles (+/- 1 day).
Experimental
PHASE 2 - ARM B: POL6326 (balixafortide) + nab-paclitaxel
MTD/RDP2 POL6326 (balixafortide) (from arm B phase Ib) will be administered over 4h intravenous infusion (biphasic regimen as detailed above/ phase Ib) followed by 100 mg/m2 nab-paclitaxel over 30 min Intravenous infusion on days 1, 8 and 15 in 28-day cycles (+/- 1 day).
Primary outcomes2
Outcomes the sponsor listed as primary.
PHASE Ib: Maximum tolerated dose (MTD) / Recommended phase II dose (RP2D) of POL6326 (balixafortide)
Time frame · 12 - 24 months
Registry description
MTD/RP2D, based on the incidence of Dose limiting toxicities (DLT) defined as the highest dose level explored at which up to one third of evaluable patients develop a DLT during the first treatment cycle.
PHASE 2: Progression free survival (PFS)
Time frame · from treatment initiation until objective tumor progression or death (at least 4.5 months)
Registry description
To assess the efficacy of POL6326 (balixafortide) in combination with either eribulin or nab-paclitaxel in terms of PFS as per RECIST v. 1.1 in patients with HER2-negative ABC.
Secondary outcomes(20)
PHASE Ib: PFS
Time frame · from treatment initiation until objective tumor progression or death (at least 4.5 months)
Registry description
To assess the efficacy of POL6326 (balixafortide) in combination with either eribulin or nab-paclitaxel in terms of PFS as per RECIST v. 1.1 in patients with HER2-negative ABC.
PHASE Ib: Overall response rate (ORR)
Time frame · from baseline until end of study (will occur when all patients have discontinued treatment or 12 month after the last patient was enrolled on the study plus the safety follow up window of 28 days after last dose of study treatment in the last patient)
Registry description
To assess the preliminary efficacy of POL6326 (balixafortide) in combination with either eribulin or nab-paclitaxel in terms of ORR defined as the proportion of patients with complete response (CR) or partial response (PR) as per RECIST v.1.1
PHASE Ib: clinical benefit rate (CBR)
Time frame · at least 6 months
Registry description
To assess the preliminary efficacy of POL6326 (balixafortide) in combination with either eribulin or nab-paclitaxel in terms of CBR, defined as the proportion of patients who obtain an objective response (CR or PR), or SD for at least 6 months for both combinations of the POL6326 (balixafortide) as per RECIST v.1.1.
PHASE IB: duration of response (DoR)
Time frame · from the first occurrence of a documented objective response to disease progression or death, up to 12 months
Registry description
To assess the preliminary efficacy of POL6326 (balixafortide) in combination with either eribulin or nab-paclitaxel in terms of DoR, defined as the time from the first occurrence of a documented objective response to disease progression or death from any cause, whichever occurs first, as per Investigator assessment using RECIST v.1.1.
PHASE Ib: maximum tumor shrinkage (MTS)
Time frame · from baseline until end of study (will occur when all patients have discontinued treatment or 12 month after the last patient was enrolled on the study plus the safety follow up window of 28 days after last dose of study treatment in the last patient
Registry description
To assess the preliminary efficacy of POL6326 (balixafortide) in combination with either eribulin or nab-paclitaxel in terms of MTS, from baseline in the size of target tumor lesions, defined as the biggest decrease, or smallest increase if no decrease observed, as per RECIST v.1.1.
PHASE 2: ORR
Time frame · from baseline until end of study (will occur when all patients have discontinued treatment or 12 month after the last patient was enrolled on the study plus the safety follow up window of 28 days after last dose of study treatment in the last patient)
Registry description
To assess the efficacy, of POL6326 (balixafortide) in combination with either eribulin or nab-paclitaxel in terms of ORR, defined as the proportion of patients with CR or PR, as per RECIST v.1.1.
PHASE 2: CBR
Time frame · at least 6 months
Registry description
To assess the efficacy, of POL6326 (balixafortide) in combination with either eribulin or nab-paclitaxel in terms of CBR, defined as the proportion of patients who obtain an objective response (CR or PR), or stable disease for at least 6 months for both combinations of the POL6326 (balixafortide) as per RECIST v.1.1.
PHASE 2: time to response (TTR)
Time frame · from treatment initiation to time of the first objective tumor response up to 12 months
Registry description
To assess the efficacy, of POL6326 (balixafortide) in combination with either eribulin or nab-paclitaxel in terms of TTR, defined as the time from treatment initiation to time of the first objective tumor response (tumor shrinkage of ≥ 30%) in patients who achieved a CR or PR, as per using RECIST v.1.1.
PHASE 2: DoR
Time frame · from the first occurrence of a documented objective response to disease progression or death, up to 12 months
Registry description
To assess the efficacy, of POL6326 (balixafortide) in combination with either eribulin or nab-paclitaxel in terms of DoR, defined as the time from the first occurrence of a documented objective response to disease progression or death from any cause, whichever occurs first, as per Investigator assessment using RECIST v.1.1.
PHASE 2: overall survival (OS)
Time frame · from baseline until end of study (will occur when all patients have discontinued treatment or 12 month after the last patient was enrolled on the study plus the safety follow up window of 28 days after last dose of study treatment in the last patient
Registry description
To assess the efficacy, of POL6326 (balixafortide) in combination with either eribulin or nab-paclitaxel in terms of OS, defined as the time from treatment initiation to death from any cause.
PHASE 2: MTS
Time frame · from baseline until end of study (will occur when all patients have discontinued treatment or 12 month after the last patient was enrolled on the study plus the safety follow up window of 28 days after last dose of study treatment in the last patient
Registry description
To assess the efficacy, of POL6326 (balixafortide) in combination with either eribulin or nab-paclitaxel in terms of MTS from baseline in the size of target tumor lesions, defined as the biggest decrease, or smallest increase if no decrease observed, as per RECIST v.1.1.
PHASE Ib/ PHASE 2: Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability] of POL6326 (balixafortide) in combination with either eribulin or nab-paclitaxel
Time frame · from baseline until end of study.All patients must be followed for AEs and SAEs for 28 days following the last dose of study drug
Registry description
Incidence and severity of AEs and SAEs according to the NCI-CTCAE v.5.0, including dose reductions, delays, and treatment discontinuations.
PHASE Ib - PHARMACOKINETICS (PK) in terms of area under the curve (AUC)
Time frame · At the end of Cycle 1 (each cycle is 28 days in POL6326 (balixafortide) - eribulin combination and 21 days in POL6326 (balixafortide) - nab paclitaxel combination)
Registry description
Plasma PK parameter AUC of POL6326 (balixafortide)
PHASE Ib - PK in terms of clearance (CL),
Time frame · At the end of Cycle 1 (each cycle is 28 days in POL6326 (balixafortide) - eribulin combination and 21 days in POL6326 (balixafortide) - nab paclitaxel combination)
Registry description
Plasma PK parameter CL of POL6326 (balixafortide)
PHASE Ib - PK in terms of distribution volume (Vd)
Time frame · At the end of Cycle 1 (each cycle is 28 days in POL6326 (balixafortide) - eribulin combination and 21 days in POL6326 (balixafortide) - nab paclitaxel combination)
Registry description
Plasma PK parameter Vd of POL6326 (balixafortide)
PHASE Ib - PK in terms of apparent half-life (t1/2)
Time frame · At the end of Cycle 1 (each cycle is 28 days in POL6326 (balixafortide) - eribulin combination and 21 days in POL6326 (balixafortide) - nab paclitaxel combination)
Registry description
Plasma PK parameter t1/2 of POL6326 (balixafortide)
PHASE Ib - PK in terms of maximal serum concentration (Cmax)
Time frame · At the end of Cycle 1 (each cycle is 28 days in POL6326 (balixafortide) - eribulin combination and 21 days in POL6326 (balixafortide) - nab paclitaxel combination)
Registry description
Plasma PK parameter Cmax of POL6326 (balixafortide)
PHASE Ib - PK in terms of trough concentrations (Ctrough)
Time frame · At the end of Cycle 1 (each cycle is 28 days in POL6326 (balixafortide) - eribulin combination and 21 days in POL6326 (balixafortide) - nab paclitaxel combination)
Registry description
Plasma PK parameter Ctrough of POL6326 (balixafortide)
PHASE Ib - PK in terms of time of maximum concentration observed (tmax)
Time frame · At the end of Cycle 1 (each cycle is 28 days in POL6326 (balixafortide) - eribulin combination and 21 days in POL6326 (balixafortide) - nab paclitaxel combination)
Registry description
Plasma PK parameter tmax of POL6326 (balixafortide)
PHASE Ib - PK in terms of time to last measurable plasma (tlast)
Time frame · At the end of Cycle 1 (each cycle is 28 days in POL6326 (balixafortide) - eribulin combination and 21 days in POL6326 (balixafortide) - nab paclitaxel combination)
Registry description
Plasma PK parameter tlast of POL6326 (balixafortide)
Posted results
Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.
No results are posted for this trial.
A trial that is still running, or that stopped early, may post results later.
Registry data comes from ClinicalTrials.gov. Study results come from studies, not from the registry. How PepBank works
Studies0
Studies that cite this trial.
No study cites this trial.
Eligibility
Who could join, as posted.
- Sex
- Female
- Age
- from 18 Years
- Healthy volunteers
- Not accepted
Inclusion and exclusion criteria, as posted
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