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Post by David Grey on Feb 26, 2019 18:04:34 GMT -5
Healthy Adults with BMI ≥ 35 Needed! Includes 5 separate stays for a total of 20 overnights & 27 outpatient visits. Home dosing is required between study visits. Act fast! See if you qualify for research study at Covance Dallas! We are recruiting healthy adults, age 18-65 with a BMI (body mass index) ≥ 35. Compensation up to $14,357 for time and participation. Also Refer Your Friends & Family Receive up to $300 per qualified referral! Covance Dallas is recruiting for Healthy Adults, Age 18-65 with a BMI (body mass in- dex) ≥ 35. Refer your friends & family to study 8390-461 and receive up to $300 per qualified referral! Call us today! - (469) 914-8330Visit us online & calculate your BMI! www.covanceclinicaltrials.com/en-us/study-details.html?caseStudyId=twtbstudy_1147399055
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Post by David Grey on Jan 23, 2019 10:15:03 GMT -5
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Post by David Grey on Jan 14, 2019 15:41:00 GMT -5
Healthy, Non-Smoking Women Needed Research Study 8398-091 is going on in your area! Covance Dallas is currently recruiting for: • Healthy, Non-Smoking Women, age 18-65 • Must be post-menopausal or surgically sterile • BMI between 18.5-35 • Join us for 2 stays of 3 overnights each, 7 outpatient visits & 1 phone call • Compensation up to $4,486 may be provided for time and participation -------------------------------------------------------------------------------- Call or visit us online today! – (469) 914-8330
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Post by David Grey on Nov 19, 2018 19:11:28 GMT -5
Call 888 989 1808 for full study details
18-65 healthy non-smoking
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Post by David Grey on Nov 19, 2018 15:15:04 GMT -5
healthy volunteer
call to find out full details as they have a bunch of new studies right now
913-370-9908
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Post by David Grey on Nov 15, 2018 9:12:03 GMT -5
Healthy, non-smoking and 18-55 years old? Avail. for 1 stay of 19 nights and 1 visit? Study #2172. Up to $4,900. Call PRA: 913-370-9908.
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Post by David Grey on Nov 15, 2018 9:11:17 GMT -5
Healthy, non-smoking and 18-55 years old? Avail. for 1 stay of 19 nights and 1 visit? Study #2172. Up to $4,900. Call PRA: 913-370-9908.
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Post by David Grey on Nov 6, 2018 17:19:00 GMT -5
A first in human phase 1 study in healthy volunteers and Granulin mutation causative of frontotemporal dementia to assess AL001 safety, tolerability, pharmacokinetics, and pharmacodynamics.
Compensation up to $2250
Call (407) 210-9839
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Post by David Grey on Oct 31, 2018 7:25:48 GMT -5
Healthy Men and Women Needed
Pharmaron, located in downtown Baltimore, is currently seeking volunteers to participate in a clinical research study to evaluate an investigational drug.
We are looking for healthy nonsmoking men and women, ages 18 to 45, who weigh more than 110.2 pounds with a BMI of between 18.5 and 30, to participate in a study consisting of one in-patient period of 38 days/ 37 nights.
Qualified participants will be compensated up to $12,260 for their time and effort.
Contact our recruiting department now at 410.706.8833
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Post by David Grey on Sept 11, 2018 10:55:41 GMT -5
Healthy Male Volunteers Needed Pharmaron, located in downtown Baltimore, is currently seeking volunteers to participate in a clinical research study to evaluate an investigational drug. We are looking for healthy men, non-smokers, ages 18 to 65, to participate in a study consisting of a 15-day/14-night inpatient stay followed 7 days later by a follow up phone call or outpatient visit. Qualified participants will be compensated up to $5,535 for their time and effort. Contact our recruiting department now at 410.706.8833 or email baltimore.recruiter@pharmaron-us.com Visit our website at www.pharmaron.com/clinical- trials/current-trials
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Post by David Grey on Sept 10, 2018 15:23:53 GMT -5
A Multicenter, Double-Blind, Randomized, Parallel-Group, Placebo-Controlled, Adaptive Dose-Finding Study to Evaluate the Efficacy and Safety of JNJ-42847922 as Adjunctive Therapy to Antidepressants in Adult Subjects With Major Depressive Dis Who Have Responded Inadequately to Antidepressant Therapy
423 West 55Th Street 4Th Floor New York, NY 10019
(212) 994-4567
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Post by David Grey on Sept 10, 2018 15:21:51 GMT -5
Frontage Clinical Services is seeking volunteers to participate in a clinical study. Males or Females should be: 18-65 years old Taking the same dose of atorvastatin (Lipitor or generic equivalent) for at least 4 weeks Study requires a screening visit of 1-2 days and then 1 visit each day for 15 days at our modern facility. Up to $3150.00 compensation for your time and travel. Ask us about our referral program!
200 Meadowlands Parkway Secaucus, NJ 07094
(877) 298-9071
View Study Website Sponsored By: Frontage Clinical Services Stipend: $3150 - $3150 Length of Study: 2 weeks Research Facility: Out-Patient Gender: Both Age: 18 - 65 Health Condition: High Cholesterol (Hyperlipidemia) More Information: 18-65 years old
Taking the same dose of atorvastatin (Lipitor or generic equivalent) for at least 4 weeks
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Post by David Grey on Sept 10, 2018 15:20:30 GMT -5
ICON Early Phase Services is conducting a research study for healthy adults ages 18 to 60.
8307 Gault Lane San Antonio, TX 78209
(210) 225-5437
The study drugs will be administered orally.
Vital signs, ECGs, physical examinations and pregnancy, drug and alcohol screens will be performed. Blood and urine samples will also be obtained during this study.
Participants will complete:
1 screening visit 16 consecutive overnights 1 outpatient visit To determine if you fully qualify, it will be necessary to obtain blood samples after a 10- hour fast. You have the option of fasting for the screening appointment, or, you may return at a later date. If ICON does not have your medical records on file, you may need to provide medical records at screening. For more information, see below.
Qualified participants may be compensated up to $4,700 for time and travel.
If you are able to answer “YES” to the following statements, you may qualify for this study.
I am a healthy adult, meaning no significant medical conditions
I am ≥ 18 and ≤ 60 years old at screening
My BMI is ≥ 18.0 and ≤ 30.0 kg/m² at screening and I weigh at least 110 lbs.
I am a non-smoker and I have abstained from tobacco or nie-containing products (e.g., cigarettes, cigars, chewing tobacco, snuff, nie patches, electronic cigarettes) for 6 months prior to screening. I agree not to smoke for the duration of the study and to abide by the rules of the clinic, which is a non-smoking facility.
I have not participated in another clinical trial of an investigational drug (or medical device) within 30 days prior to screening and I am not currently participating in another trial of an investigational drug (or medical device)
If Female, I am not pregnant or breastfeeding
If Female and not capable of becoming pregnant, I have been postmenopausal for at least 2 years or I am surgically sterile (ovaries removed, tubes tied, uterus removed)
If Male and I have a partner capable of becoming pregnant, I agree to a highly effective od of birth control during the study and for 3 months following last drug dose. ods of birth control for you and your partner will be discussed at screening.
If Male, I agree not to donate sperm during the study and for 3 months following last drug dose
I am able to communicate effectively in English with the study personnel
I do not have a history or presence of clinically significant allergic (except for untreated, asymptomatic, seasonal allergies at dosing), hematological, endocrine, pulmonary, gastrointestinal, cardiovascular, renal, hepatic, psychiatric, or neurological disease
I have not had previous gastrointestinal surgery such as the removal of parts of the stomach, bowel, liver, or pancreas
I do not have a history of surgery or major trauma within 12 weeks of screening and I do not have surgery planned during the study
I do not have evidence of atrial fibrillation, atrial flutter, complete bundle branch block, Wolf‑Parkinson‑White Syndrome, or a cardiac pacemaker
I do not have known personal or family history of a congenital long QT syndrome (LQTS) heart condition or known family history of sudden death
I do not have a history of alcohol abuse, illicit drug use, significant mental illness, or physical dependence to any opioid
I do not have an allergy to moxifloxacin or any fluoroquin antibiotics
I do not have a history of heart problems (i.e., history of torsade de pointes, prolongation, proarrhythmic conditions such as clinically significant bradycardia or acute myocardial ischemia, hypokalemia, or hypomagnesemia)
I do not have a history of history of tendon diss (i.e., tendinitis or tendon rupture, peripheral neuropathy, suspected central nervous system diss)
I have not taken any prescription medications or over-the-counter (OTC) drugs (including herbal preparations or dietary supplements), or any drugs that induce or inhibit the study drug within 14 days of check-in, or that require uing use during study participation
I do not use or have used any prescription medication or OTC drug (including herbal preparations or dietary supplements ) that prolong the heart’s QT/QTc interval within 14 days prior to check-in, or that require uing use during sturdy participation
I do not consume more than 4 cups of coffee daily and I am willing to abstain from consuming caffeine or xanthine-containing products (e.g., tea, coffee, chocolate, cola, etc.) from 48 hours prior to first dose until the end of the study
I am willing to abstain from consuming alcohol from 48 hours prior to first dose until the end of the study
I am willing to abstain from consuming grapefruit and/or grapefruit juice within 14 days prior to check-in and I am willing to abstain from consumption of grapefruit and/or grapefruit juice until the end of the study
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Post by David Grey on Sept 10, 2018 15:18:56 GMT -5
For more information or to find out if you may qualify, call 913-210-5588 today!
9755 Ridge Dr. Lenexa, KS 66219
(913) 210-5588
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Post by David Grey on Sept 10, 2018 15:17:48 GMT -5
Pharmaron in downtown Baltimore is seeking women age 18+, to participate in a clinical study of an investigational injectable for cellulite.
800 W. Baltimore Street Baltimore, MD 21201
(410) 706-8833
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