Lesson 25

Lesson 25

University

8 Qs

quiz-placeholder

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Lesson 25

Lesson 25

Assessment

Quiz

Health Sciences

University

Easy

Created by

Javier Gomez-Ambrosi

Used 2+ times

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8 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

10 sec • 5 pts

1. What type of clinical trial was used?

Phase 1b, randomized, double-blind

Phase 2, non-randomized, uncontrolled, single-blind

Phase 1b, randomized, placebo-controlled, single-blind

Phase 2, randomized, placebo-controlled, double-blind

2.

MULTIPLE CHOICE QUESTION

10 sec • 5 pts

2. What was the primary endpoint?

Appetite and cachexia symptoms

Change from baseline in body weight

Digital measures of physical activity

Safety

3.

MULTIPLE CHOICE QUESTION

10 sec • 5 pts

3. Which group had a median difference of 2.81 kg of weight gain as compared to the placebo group?

Ponsegromab 100 mg

Ponsegromab 200 mg

Ponsegromab 400 mg

All the ponsegromab groups

4.

MULTIPLE CHOICE QUESTION

10 sec • 5 pts

4. How many patients experienced adverse effects of any cause?

80% in the ponsegromab groups and 70% in the placebo group

22 to 40% in the ponsegromab groups and 24% in the placebo group

4 to 11% in the ponsegromab groups and 9% in the placebo group

67 to 74% in the ponsegromab groups and 80% in the placebo group

5.

MULTIPLE CHOICE QUESTION

10 sec • 5 pts

5. What type of clinical trial was used?

Phase 2b randomized, double-blind, placebo-controlled trial

Phase 2a randomized, double-blind, uncontrolled trial

Phase 2a randomized, double-blind, placebo-controlled trial

Phase 2a randomized, single-blind, placebo-controlled trial

6.

MULTIPLE CHOICE QUESTION

10 sec • 5 pts

6. What was the primary endpoint?

Relative liver fat change

Change in body weight change at 24 weeks

Change in insulin sensitivity and lipid metabolism

Change in visceral adipose tissue

7.

MULTIPLE CHOICE QUESTION

10 sec • 5 pts

7. The relative percentage of hepatic fat fraction in the 8 mg RETA at 48 weeks was?

-57.0%

-81.4%

-81.7%

-86.0%

8.

MULTIPLE CHOICE QUESTION

10 sec • 5 pts

8. Which answer is INCORRECT?

The safety profile of retatrutide in people with MASLD was similar to that observed previous trials of people with obesity

There were no hepatotoxicity signals in the overall obesity trial population or in the subset of participants with MASLD through 48 weeks

Several cases of patients with advanced fibrosis or cirrhosis in the group with the higher doses of RETA were reported

Mild-to-moderate gastrointestinal events were the most frequently reported adverse events