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Hormone Therapy

Tamoxifen for Tumors (HORMONET Trial)

Phase 2
Waitlist Available
Led By Jonathan R Strosberg, MD
Research Sponsored by AC Camargo Cancer Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through study completion, an average of 5 years
Awards & highlights

HORMONET Trial Summary

This trialwill study if Tamoxifen can help patients with neuroendocrine tumors and positive hormone expression.

Eligible Conditions
  • Tumors
  • Neuroendocrine Tumors

HORMONET Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion, an average of 5 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and through study completion, an average of 5 years for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Secondary outcome measures
Disease control rate
Incidence of Treatment-related Adverse Events
Progression-free survival
+2 more
Other outcome measures
CTC positivity rate
PET-CT gallium-68 intake variation
PET-CT gallium-68 number variation

HORMONET Trial Design

1Treatment groups
Experimental Treatment
Group I: TamoxifenExperimental Treatment1 Intervention
The participants will receive tamoxifen 20mg orally once daily with a glass of water. Each cycle will be defined for 42 days (6 weeks).
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Tamoxifen
2005
Completed Phase 4
~30070

Find a Location

Who is running the clinical trial?

AC Camargo Cancer CenterLead Sponsor
27 Previous Clinical Trials
7,998 Total Patients Enrolled
H. Lee Moffitt Cancer Center and Research InstituteOTHER
542 Previous Clinical Trials
135,469 Total Patients Enrolled
1 Trials studying Tumors
9 Patients Enrolled for Tumors
Jonathan R Strosberg, MDPrincipal InvestigatorH. Lee Moffitt Cancer Center and Research Institute

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

What conditions does Tamoxifen usually address?

"Tamoxifen is a well-known treatment option for malignant neoplasms, ovarian cancer, and ovulation induction therapy."

Answered by AI

What adverse effects might be associated with Tamoxifen use?

"Tamoxifen has been awarded a safety rating of 2, as Phase 2 trials indicate the presence of some data points suggesting it is safe yet there are no evidentiary claims that its efficacy can be proven."

Answered by AI

Is this clinical investigation recruiting participants?

"Per the information displayed on clinicaltrials.gov, this particular trial is not actively seeking enrolment. It was initially posted in March 13th 2019 and last edited January 13rd 2023. However, there are a plethora of other studies currently recruiting participants - 2511 to be exact!"

Answered by AI

What other experiments regarding the efficacy of Tamoxifen have been conducted thus far?

"At this time, 69 studies are utilizing Tamoxifen as an experimental treatment with 22 of them being in their final stage. Most trials focused on the drug take place within Oregon and Ohio but there is a far reach with 7552 sites hosting related clinical trials."

Answered by AI

What is the utmost capacity of participants for this research project?

"This clinical trial is not presently enrolling new patients. It was originally posted on March 13th, 2019 and last updated on January 13th, 2023. If you are seeking alternative studies to participate in, there are currently 2442 active trials recruiting for those with progesterone receptor positive tumors; additionally, 69 trials using Tamoxifen have open enrolment slots available too."

Answered by AI
Recent research and studies
~4 spots leftby Apr 2025