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Lesson 25

Total questions: 8

Worksheet time: 80secs

Name
Class
Date
1.

1. What type of clinical trial was used?

a)

Phase 1b, randomized, double-blind

b)

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

c)

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

d)

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

2.

2. What was the primary endpoint?

a)

Appetite and cachexia symptoms

b)

Change from baseline in body weight

c)

Digital measures of physical activity

d)

Safety

3.

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

a)

Ponsegromab 100 mg

b)

Ponsegromab 200 mg

c)

Ponsegromab 400 mg

d)

All the ponsegromab groups

4.

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

a)

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

b)

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

c)

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

d)

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

5.

5. What type of clinical trial was used?

a)

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

b)

Phase 2a randomized, double-blind, uncontrolled trial

c)

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

d)

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

6.

6. What was the primary endpoint?

a)

Relative liver fat change

b)

Change in body weight change at 24 weeks

c)

Change in insulin sensitivity and lipid metabolism

d)

Change in visceral adipose tissue

7.

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

a)

-57.0%

b)

-81.4%

c)

-81.7%

d)

-86.0%

8.

8. Which answer is INCORRECT?

a)

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

b)

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

c)

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

d)

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