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HIPAA Compliant
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Completed

Phase 1
All Genders
ID00005883

A Phase I - Part B Multiple Dose Trial of Phenethyl Isothiocyanate

Led by NYU Langone Health · Updated on 2011-03-28

N/A

Participants Needed

N/A

Research Sites

N/A

Total Duration

On this page

Sponsors

N

NYU Langone Health

Lead Sponsor

N

National Cancer Institute (NCI)

Collaborating Sponsor

AI-Summary

What this Trial Is About

RATIONALE: Chemoprevention therapy is the use of certain drugs to try to prevent the development or recurrence of cancer. Phenethyl isothiocyanate may be effective in preventing lung cancer in smokers. PURPOSE: Phase I trial of phenethyl isothiocyanate in preventing lung cancer in people who smoke.

CONDITIONS

Brief Title

Phenethyl Isothiocyanate in Preventing Lung Cancer in People Who Smoke

Who Can Participate

All Genders

Eligibility Criteria

DISEASE CHARACTERISTICS: Asymptomatic smokers who either refuse to or cannot stop smoking Urinary cotinine levels greater than 100 ng/mL Willing to adhere to certain dietary restrictions limiting intake of cruciferous vegetables (watercress, broccoli, radishes, mustard, brussels sprouts) while on study

PATIENT CHARACTERISTICS: Age: Not specified Performance status: Not specified Life expectancy: Not specified Hematopoietic: WBC at least 3,500/mm3 Platelet count at least 100,000/mm3 Hepatic: Bilirubin less than 1.6 mg/dL Transaminases less than 2 times normal Renal: Creatinine less than 1.6 mg/dL Urinary RBC levels 0-2 Urinary WBC levels at least 0-2 Pulmonary: No dyspnea at rest Other: No concurrent illness, condition, or symptom that would preclude study Not pregnant or nursing Negative pregnancy test Fertile patients must use effective contraception

PRIOR CONCURRENT THERAPY: Not specified

Trial Site Locations

Site Locations not provided

Location information for this trial is currently unavailable.

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