ACROBAT Edge: Safety and Efficacy of Switching Injected SRLs to Oral Paltusotine in Patients With Acromegaly

Author:

Gadelha Monica R1ORCID,Gordon Murray B2,Doknic Mirjana3,Mezősi Emese4,Tóth Miklós5,Randeva Harpal67,Marmon Tonya8,Jochelson Theresa8,Luo Rosa8,Monahan Michael8,Madan Ajay8,Ferrara-Cook Christine8,Struthers R Scott8,Krasner Alan8

Affiliation:

1. Neuroendocrinology Research Center/Endocrinology Division, Medical School and Hospital Universitario Clementino Fraga Filho, Universidade Federal do Rio de Janeiro , Rio de Janeiro, CEP 21941-913 , Brazil

2. Allegheny Neuroendocrinology Center, Division of Endocrinology, Allegheny General Hospital , Pittsburgh, Pennsylvania 15212 , USA

3. Neuroendocrine Department, Clinic for Endocrinology, Diabetes and Metabolic Diseases, University Clinical Center of Serbia; Faculty of Medicine, University of Belgrade , Belgrade 11000 , Serbia

4. First Department of Internal Medicine, Faculty of Medicine , University of Pécs Medical School, Pécs 7624 , Hungary

5. Department of Internal Medicine and Oncology, Faculty of Medicine , Semmelweis University, Budapest 1085 , Hungary

6. Warwickshire Institute for the Study of Diabetes, Endocrinology and Metabolism (WISDEM) , University Hospitals Coventry and Warwickshire NHS Trust, Coventry CV2 2DX , UK

7. Division of Biomedicine, Warwick Medical School, University of Warwick , Coventry CV4 7AL , UK

8. Crinetics Pharmaceuticals Inc , San Diego, California 92121 , USA

Abstract

Abstract Context Paltusotine is a once-daily, oral, nonpeptide small-molecule somatostatin receptor type 2 (SST2) agonist in clinical development for treatment of acromegaly. Objective This work aimed to evaluate change in insulin-like growth factor I (IGF-I) levels in patients switched from octreotide long-acting release or lanreotide depot monotherapy to paltusotine. Methods A phase 2, open-label, prospective, multicenter, multinational, nonrandomized, single-arm exploratory study was conducted in which dosage uptitrations were performed in a double-blinded manner. At 26 global sites, patients with acromegaly switched to paltusotine from injected somatostatin receptor ligand (SRL)-based therapy. Patients received 13-week treatment with once-daily oral paltusotine (10-40 mg/d). The primary end point was change from baseline to week 13 in IGF-I for patients who switched from long-acting octreotide or lanreotide depot monotherapy to paltusotine (group 1). All patients underwent a 4-week paltusotine washout at end of treatment period (wk 13-17). IGF-I, growth hormone (GH), patient-reported outcome, and safety data were collected. Results Forty-seven patients enrolled. In group 1 (n = 25), IGF-I and GH showed no significant change between SRL baseline and end of paltusotine treatment at week 13 (median change in IGF-I = −0.03×upper limit of normal [ULN]; P = .6285; GH = −0.05 ng/mL; P = .6285). IGF-I and GH rose significantly in the 4 weeks after withdrawing paltusotine (median change in IGF-I = 0.55×ULN; P < .0001 [median increase 39%]; GH = 0.72 ng/mL; P < .0001 [109.1% increase]). No patients discontinued because of adverse events (AE); no treatment-related serious AEs were reported. Conclusion These results suggest once-daily oral paltusotine was effective in maintaining IGF-I values in patients with acromegaly who switched from injected SRLs. Paltusotine was well tolerated with a safety profile consistent with other SRLs.

Funder

Crinetics Pharmaceuticals

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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