PeptideTrace
Research CompoundPorcine Vasopressin Analogue (Withdrawn)

Lypressin

Diapid

C

Evidence Grade C — Moderate human evidence. 24 published studies, 17 human. 85 registered clinical trials.

85 trials24 studiesUSEUCA

Overview

Lypressin (lysine vasopressin) is a synthetic version of the natural pig form of vasopressin. It was previously sold as a nasal spray (Diapid) for diabetes insipidus but was voluntarily withdrawn from the market around 1997 — not for safety reasons, but because desmopressin offered a clearly better clinical profile with longer duration and fewer side effects.

Research Activity

24studies
Human 17
Animal 5
In-vitro 1
Reviews 4

24 published studies: 17 human, 5 animal, 1 in-vitro, 4 reviews

Regulatory Status

US
Not approved by FDA(FDA)
EU
Not authorised by EMA(EMA)
CA
Not approved by Health Canada(Health Canada)

Legal Status

USNot applicable (not approved)
EUNot applicable (not authorised)
CANot applicable (not approved)

Summary

Lypressin was previously marketed as Diapid (Sandoz) nasal spray for diabetes insipidus. It was voluntarily withdrawn from the market around 1997, not for safety or efficacy reasons, but because desmopressin offered a superior clinical profile: longer duration of action, greater selectivity for kidney receptors, minimal blood pressure effects, and multiple formulation options.

Lypressin is of historical interest as an early synthetic hormone replacement but has no current clinical role.

Mechanism of Action

Lypressin acts on the same vasopressin receptors as the human hormone, promoting water reabsorption in the kidneys. It differs from human vasopressin at a single amino acid position (lysine instead of arginine at position 8). Its short duration of action (3–4 hours) and non-selective receptor profile — causing blood vessel constriction alongside the desired kidney effects — made it clinically inferior to desmopressin.

Research Summary

Lypressin is of historical interest only. Its short duration of action (3-4 hours) and non-selective receptor profile — causing blood vessel constriction alongside the desired kidney effects — made it clinically inferior to desmopressin in every meaningful way. No current clinical role exists. It retains minor relevance as a pharmacological research tool for studying vasopressin receptor subtypes. No active development programmes exist.

Clinical Trials

NCT07304466N/ANot Yet Recruiting

Effects of Terlipressin and Somatostatin on Portal Pressure in Patients Undergoing Living Donor Liver Transplantation

Istanbul Medipol University HospitalEndpoint: Decrease in portal pressure by 20% from the baselineCompletion: 2027-03-30
NCT07252401N/ANot Yet Recruiting

Terlipressin vs. Somatostatin in Cirrhotic Patients With Acute Gastrointestinal Bleeding and Acute Kidney Injury

General Hospital of Shenyang Military RegionEndpoint: Reversal of AKICompletion: 2028-03-31
NCT07460908N/ACompleted

Comparison of Terlipressin Versus Octreotide in Patients With Hepatorenal Syndrome

Lahore General HospitalEndpoint: Treatment response based on serum creatinine at 48 hoursCompletion: 2025-10-30
NCT06855758N/ARecruiting

Effect of Terlipressin for Intraoperative Blood Pressure Management in Kidney Transplantation

Beijing Friendship HospitalEndpoint: Delayed graft functionCompletion: 2027-06-01
NCT06556472N/ANot Yet Recruiting

Safety and Efficacy of Continuous Infusion of Terlipressin With Norepinephrine Versus Norepinephrine Alone in Improving Outcomes of Acute Kidney Injury in Acute on Chronic Liver Failure With Septic Shock

Institute of Liver and Biliary Sciences, IndiaEndpoint: Proportion of patients developing 1 stage improvement in Acute kidney injury stage with resolution of shock at day 4 in both groupsCompletion: 2025-08-31
View all 85 trials on ClinicalTrials.gov →

The information on this page is provided for educational and research reference purposes only. This is not medical advice. Always consult a qualified healthcare professional before making any health-related decisions.

Related Compounds

Exenatide

Approved
GLP-1 Receptor Agonist

Exenatide was the first GLP-1 receptor agonist approved anywhere, reaching the market as Byetta in April 2005. The once-weekly formulation Bydureon followed in 2012. Clinical trials showed blood sugar reductions (HbA1c) of 1.6–1.9% and modest weight loss of 2–4 kg. The EXSCEL cardiovascular outcomes trial, involving over 14,700 patients, showed a trend toward cardiovascular benefit but narrowly missed statistical significance. While exenatide was groundbreaking as the first in its class, it has been largely overtaken by newer GLP-1 treatments that offer greater efficacy, less frequent dosing, and proven cardiovascular benefits. It remains available and in clinical use, particularly in combination products.

Lixisenatide

Approved
GLP-1 Receptor Agonist

Lixisenatide was marketed as Adlyxin in the US (approved July 2016), though it has since been discontinued in the US market. The ELIXA cardiovascular trial, involving over 6,000 patients, was the first cardiovascular outcomes trial for any GLP-1 medication to report results. It showed a neutral cardiovascular profile — neither harmful nor beneficial — meeting safety requirements but not demonstrating the heart benefits later shown by semaglutide and liraglutide. Lixisenatide found its primary clinical role in combination with basal insulin, marketed as Soliqua (lixisenatide plus insulin glargine). This combination addresses both fasting blood sugar (via insulin) and post-meal spikes (via lixisenatide) in a single daily injection. As a standalone treatment, it has been largely superseded by more potent GLP-1 medications.

Pramlintide

Approved
Amylin Analogue

Pramlintide is marketed as Symlin (approved March 2005) and remains the only approved amylin-based treatment. It is used alongside mealtime insulin in both type 1 and type 2 diabetes. Clinical trials showed modest blood sugar improvements (HbA1c reductions of 0.2–0.6%) and approximately 2.3 kg of weight loss — less dramatic than GLP-1 treatments but meaningful as an add-on therapy. Symlin carries a boxed warning for severe hypoglycaemia, particularly when combined with insulin, and requires careful dose adjustment. Practical uptake has been limited by the need for separate injections at each meal alongside existing insulin injections. Despite its modest clinical impact, pramlintide remains the only medication that addresses the amylin deficiency in diabetes, filling a distinct biological role that GLP-1 treatments do not cover.