US-based biopharmaceutical firm Amgen has reported positive results from its second placebo-controlled phase three trial of AMG 416 to treat secondary hyperparathyroidism (SHPT) in patients with chronic kidney disease (CKD).

The company said that the 26-week, randomised, double-blind, placebo-controlled trial met all primary and secondary endpoints.

Discover B2B Marketing That Performs

Combine business intelligence and editorial excellence to reach engaged professionals across 36 leading media platforms.

Find out more

The trial evaluated the efficacy and safety of AMG 416 to treat SHPT in 508 patients with CKD receiving haemodialysis.

In the trial, patients were given AMG 416 or a placebo three times a week by intravenous injection with each haemodialysis treatment, while doses ranged from a minimum of 2.5mg to a maximum of 15mg.

"AMG 416 could become an important new treatment option for dialysis patients with secondary hyperparathyroidism."

Patients were also given a standard of care which could include calcium supplements, vitamin D sterols and phosphate binders, if prescribed by the individual physician.

The trial’s primary endpoint was the proportion of patients with greather than 30% reduction from the baseline in parathyroid hormone (PTH) levels during an efficacy assessment phase (EAP), defined as the period between weeks 20 and 27.

GlobalData Strategic Intelligence

US Tariffs are shifting - will you react or anticipate?

Don’t let policy changes catch you off guard. Stay proactive with real-time data and expert analysis.

By GlobalData

In the AMG 416 group, 74% of patients achieved a greater than 30% reduction from baseline in PTH, compared with 8.3% in the placebo arm, marking a statistically significant result.

Secondary endpoints of the trial included the percent change from baseline during the EAP in serum phosphorus (P) concentration and corrected calcium (cCa) concentration.

The company said that both secondary endpoint results were statistically significant.

Amgen executive vice-president of research and development Sean Harper said: "The results from this second phase three study help to confirm that AMG 416 could become an important new treatment option for dialysis patients with secondary hyperparathyroidism.

"Despite the variety of options available for the treatment of this disease, an unmet need remains for an intravenous therapy that can be administered along with haemodialysis.

"We look forward to sharing results of a head-to-head study evaluating AMG 416 compared to cinacalcet next year."

The results follow the recent announcement of positive data from a prior placebo-controlled phase three trial of AMG 416, which was similar in design and size.

Clinical Trials Arena Excellence Awards - Nominations Closed

Nominations are now closed for the Clinical Trials Arena Excellence Awards. A big thanks to all the organisations that entered – your response has been outstanding, showcasing exceptional innovation, leadership, and impact.

Excellence in Action
Recognised with 2025 Excellence Awards for Research and Development and Marketing , Novotech converted FDA/EMA fast track designations into faster HDV trial timelines while translating complex HBV science into sponsor ready insights. Discover how this dual strength in execution and communication is reshaping liver disease clinical development.

Discover the Impact