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NCT03737370CompletedPhase 1

Fractionated Docetaxel and Radium 223 in Metastatic Castration-Resistant Prostate Cancer

A Phase I Trial of Fractionated Docetaxel and Radium 223 in Metastatic Castration-Resistant Prostate Cancer (CRPC)

Source: ClinicalTrials.gov · Last updated 7 Oct 2025

Brief summary (registry, in English)

The objective of this study is to determine the maximum safe dose of Ra-223 in combination with fractionated (split doses) docetaxel when given to subjects and to determine the best administering dose. The study will look at side effects that may happen while taking the combination treatment. A total of approximately 18 subjects will take part in the dose escalation part of the study and an additional 25 subjects will participate in the expansion cohort. This study will be conducted across four centers in the United States.

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
43 (actual)
First submitted
25 Oct 2018
Start date
30 Jan 2018
Primary completion date
31 Dec 2024
Lead sponsor
Tufts Medical Center
NCT number
NCT03737370

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 43
  • From 30 Jan 2018 to the primary completion date, 31 Dec 2024
  • 4 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior radionuclide therapy for CRPC
  • Prior docetaxel for CRPC. (Permitted if given for castration sensitive disease \> 6 months prior).
  • Concurrent enrollment in any other investigational anticancer therapy
  • Treatment with any myelosuppressive agent within 30 days of enrollment
  • Evidence of neuroendocrine or small cell differentiation on prior biopsy

Other illness

  • Antiandrogen therapy within 4 weeks of enrollment. However, patients with primary failure of secondary anti-androgen therapy OR symptomatic progression, objective progression and/or biochemical evidence of rising PSA less than 4 weeks after discontinuation of anti-androgen therapy will not have anti-androgen withdrawal responses and will not be excluded.
  • Other serious medical condition as judged by the investigator.
  • Active second malignancy that requires therapy.
  • History of severe hypersensitivity reactions to docetaxel or to drugs formulated with polysorbate 80

Other

  • Preexisting peripheral neuropathy grade 2 or higher.
  • Known brain or leptomeningeal metastases
  • Presence of bulky visceral metastases, defined as any of the following:
    • ≥ 4 lung lesions (at least 1cm each in size in the longest diameter) or pulmonary lymphangitic metastasis
    • Liver metastases with sum of lesion diameters totaling ≥ 5cm

Who the study is looking for

  • Histologically or cytologically confirmed adenocarcinoma of the prostate
  • Documented metastatic castration resistant disease with PSA progression, radiographic progression, or both, despite medical or surgical castration
  • Two or more bone metastases detected on skeletal scintigraphy
  • Eligible for docetaxel chemotherapy
  • ECOG Performance Status 0-2
  • Adequate organ function:
    • Hemoglobin \> 10 g/dL
    • Absolute Neutrophil Count ≥ 1,500 K/mL
    • Platelet count ≥ 150,000 x 10\^9/L
    • Total bilirubin ≤ 1.5x upper limit of normal range, excluding Gilbert syndrome
    • Serum AST ≤ 1.5 x upper limit of normal range
    • Serum ALT ≤ 1.5 x upper limit of normal range
  • Estimated glomerular filtration rate (GFR) \> 30mL/min
  • Ongoing castration (androgen deprivation therapy or prior orchiectomy)
  • Male subjects with female sexual partners of childbearing potential must agree to use at least one highly effective methods of birth control.
  • Ability to understand and willingness to sign an informed consent form prior to initiation of any study procedures.
  • Age ≥ 18 years

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Lahey Hospital & Medical Center
Coordinator of this site? Confirm its status
BostonUnited StatesUnknown status
Tufts Medical Center
Coordinator of this site? Confirm its status
BostonUnited StatesUnknown status
Ohio State University Comprehensive Cancer Center
Coordinator of this site? Confirm its status
ColumbusUnited StatesUnknown status
Henry Ford Health System
Coordinator of this site? Confirm its status
DetroitUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.