Procalamine

Hyperphosphataemia, Communicable Diseases, Dialysis therapy + 4 more

Treatment

3 FDA approvals

3 Active Studies for Procalamine

What is Procalamine

Calcium acetate

The Generic name of this drug

Treatment Summary

Valine is an important amino acid that helps with muscle growth and tissue repair. It also has stimulant properties and is used in the production of antibiotics.

ProcalAmine

is the brand name

image of different drug pills on a surface

Procalamine Overview & Background

Brand Name

Generic Name

First FDA Approval

How many FDA approvals?

ProcalAmine

Calcium acetate

1982

77

Approved as Treatment by the FDA

Calcium acetate, otherwise known as ProcalAmine, is approved by the FDA for 3 uses which include Kidney Failure, Chronic and End-stage Renal Failure (ESRF) .

Kidney Failure, Chronic

Helps manage End-stage Renal Failure (ESRF)

End-stage Renal Failure (ESRF)

Helps manage End-stage Renal Failure (ESRF)

Hyperphosphataemia

Helps manage Hyperphosphataemia

Effectiveness

How Procalamine Affects Patients

L-valine is an essential amino acid, which helps build and repair muscles. It also works to lower blood sugar levels and increase growth hormone production. It is important for children's growth and adults' overall health. When taken as a supplement, it is best to combine it with isoleucine and leucine in the ratio of 2:1:2. Without enough L-valine in your diet, you may experience slowed growth, neurological issues, or anemia. It is used in both the pharmaceutical and food industries.

How Procalamine works in the body

Valine, Leucine and Isoleucine are essential amino acids that humans cannot produce, so they must be consumed in the diet. These three amino acids are broken down in muscles, producing energy that is used to make ATP. All three use the same two enzymes in the first two steps of breakdown, then their pathways diverge. Valine is turned into a glucogenic compound, while Isoleucine is both glucogenic and ketogenic. Leucine is converted into ketogenic compounds. When these pathways are disrupted, it is called Maple Syrup Urine Disease and can lead to mental retardation and poor myelin

When to interrupt dosage

The advocated measure of Procalamine is contingent upon the diagnosed state, which may include amino acid supplementation, Encephalopathies and Uremic Encephalopathy. The amount of dosage also relies on the technique of delivery (e.g. Intravenous or Solution - Intravenous) detailed in the following table.

Condition

Dosage

Administration

Hyperphosphataemia

667.0 mg, , 667.0 mg/mL, 0.839 mg/mg, 0.952 mg/mg, 952.0 mg, 5.95 mg/mL, 450.0 mg, 300.0 mg, 668.0 mg, 0.26 mg/mL, 22.0 mg/mL, 6.67 mg/mg, 44.0 mg/mL

, Oral, Tablet - Oral, Tablet, Capsule - Oral, Capsule, Solution, Solution - Oral, Powder, for solution - Topical, Topical, Powder, for solution, Solution - Topical, Injection - Intravenous, Intravenous, Injection, solution, concentrate - Intravenous, Liquid, Liquid - Intravenous, Injection, solution, concentrate, Tablet, coated - Oral, Solution - Intravenous, Injection, Tablet, coated

Kidney

667.0 mg, , 667.0 mg/mL, 0.839 mg/mg, 0.952 mg/mg, 952.0 mg, 5.95 mg/mL, 450.0 mg, 300.0 mg, 668.0 mg, 0.26 mg/mL, 22.0 mg/mL, 6.67 mg/mg, 44.0 mg/mL

, Oral, Tablet - Oral, Tablet, Capsule - Oral, Capsule, Solution, Solution - Oral, Powder, for solution - Topical, Topical, Powder, for solution, Solution - Topical, Injection - Intravenous, Intravenous, Injection, solution, concentrate - Intravenous, Liquid, Liquid - Intravenous, Injection, solution, concentrate, Tablet, coated - Oral, Solution - Intravenous, Injection, Tablet, coated

high phosphate levels

667.0 mg, , 667.0 mg/mL, 0.839 mg/mg, 0.952 mg/mg, 952.0 mg, 5.95 mg/mL, 450.0 mg, 300.0 mg, 668.0 mg, 0.26 mg/mL, 22.0 mg/mL, 6.67 mg/mg, 44.0 mg/mL

, Oral, Tablet - Oral, Tablet, Capsule - Oral, Capsule, Solution, Solution - Oral, Powder, for solution - Topical, Topical, Powder, for solution, Solution - Topical, Injection - Intravenous, Intravenous, Injection, solution, concentrate - Intravenous, Liquid, Liquid - Intravenous, Injection, solution, concentrate, Tablet, coated - Oral, Solution - Intravenous, Injection, Tablet, coated

Astringent

667.0 mg, , 667.0 mg/mL, 0.839 mg/mg, 0.952 mg/mg, 952.0 mg, 5.95 mg/mL, 450.0 mg, 300.0 mg, 668.0 mg, 0.26 mg/mL, 22.0 mg/mL, 6.67 mg/mg, 44.0 mg/mL

, Oral, Tablet - Oral, Tablet, Capsule - Oral, Capsule, Solution, Solution - Oral, Powder, for solution - Topical, Topical, Powder, for solution, Solution - Topical, Injection - Intravenous, Intravenous, Injection, solution, concentrate - Intravenous, Liquid, Liquid - Intravenous, Injection, solution, concentrate, Tablet, coated - Oral, Solution - Intravenous, Injection, Tablet, coated

Communicable Diseases

667.0 mg, , 667.0 mg/mL, 0.839 mg/mg, 0.952 mg/mg, 952.0 mg, 5.95 mg/mL, 450.0 mg, 300.0 mg, 668.0 mg, 0.26 mg/mL, 22.0 mg/mL, 6.67 mg/mg, 44.0 mg/mL

, Oral, Tablet - Oral, Tablet, Capsule - Oral, Capsule, Solution, Solution - Oral, Powder, for solution - Topical, Topical, Powder, for solution, Solution - Topical, Injection - Intravenous, Intravenous, Injection, solution, concentrate - Intravenous, Liquid, Liquid - Intravenous, Injection, solution, concentrate, Tablet, coated - Oral, Solution - Intravenous, Injection, Tablet, coated

Dialysis therapy

667.0 mg, , 667.0 mg/mL, 0.839 mg/mg, 0.952 mg/mg, 952.0 mg, 5.95 mg/mL, 450.0 mg, 300.0 mg, 668.0 mg, 0.26 mg/mL, 22.0 mg/mL, 6.67 mg/mg, 44.0 mg/mL

, Oral, Tablet - Oral, Tablet, Capsule - Oral, Capsule, Solution, Solution - Oral, Powder, for solution - Topical, Topical, Powder, for solution, Solution - Topical, Injection - Intravenous, Intravenous, Injection, solution, concentrate - Intravenous, Liquid, Liquid - Intravenous, Injection, solution, concentrate, Tablet, coated - Oral, Solution - Intravenous, Injection, Tablet, coated

Kidney Failure, Chronic

667.0 mg, , 667.0 mg/mL, 0.839 mg/mg, 0.952 mg/mg, 952.0 mg, 5.95 mg/mL, 450.0 mg, 300.0 mg, 668.0 mg, 0.26 mg/mL, 22.0 mg/mL, 6.67 mg/mg, 44.0 mg/mL

, Oral, Tablet - Oral, Tablet, Capsule - Oral, Capsule, Solution, Solution - Oral, Powder, for solution - Topical, Topical, Powder, for solution, Solution - Topical, Injection - Intravenous, Intravenous, Injection, solution, concentrate - Intravenous, Liquid, Liquid - Intravenous, Injection, solution, concentrate, Tablet, coated - Oral, Solution - Intravenous, Injection, Tablet, coated

Warnings

Procalamine Contraindications

Condition

Risk Level

Notes

Hypercalcemia

Do Not Combine

Pulse Frequency

Do Not Combine

There are 20 known major drug interactions with Procalamine.

Common Procalamine Drug Interactions

Drug Name

Risk Level

Description

Technetium Tc-99m oxidronate

Major

Calcium acetate may decrease effectiveness of Technetium Tc-99m oxidronate as a diagnostic agent.

Dobutamine

Minor

The therapeutic efficacy of Dobutamine can be decreased when used in combination with Calcium acetate.

3-Aza-2,3-Dihydrogeranyl Diphosphate

Moderate

Calcium acetate can cause a decrease in the absorption of 3-Aza-2,3-Dihydrogeranyl Diphosphate resulting in a reduced serum concentration and potentially a decrease in efficacy.

Acebutolol

Moderate

The therapeutic efficacy of Acebutolol can be decreased when used in combination with Calcium acetate.

Acetyldigitoxin

Moderate

Calcium acetate may increase the arrhythmogenic and cardiotoxic activities of Acetyldigitoxin.

Procalamine Toxicity & Overdose Risk

Taking too much of branched-chain amino acids (BCAAs) can lead to dangerously low blood sugar levels and a higher risk of death in those with ALS.

Procalamine Novel Uses: Which Conditions Have a Clinical Trial Featuring Procalamine?

At present, no active trials are investigating the potential of Procalamine to address Uremic Encephalopathy, Encephalopathies and Hepatic coma.

Condition

Clinical Trials

Trial Phases

high phosphate levels

0 Actively Recruiting

Kidney Failure, Chronic

0 Actively Recruiting

Communicable Diseases

0 Actively Recruiting

Hyperphosphataemia

0 Actively Recruiting

Dialysis therapy

3 Actively Recruiting

Not Applicable, Phase 3, Phase 4

Astringent

0 Actively Recruiting

Kidney

0 Actively Recruiting

Patient Q&A Section about procalamine

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

What is ProcalAmine used for?

"ProcalAmine is a medication indicated for adults who are mildly catabolic and require short-term parenteral nutrition. It is used to preserve body protein and improve nitrogen balance."

Answered by AI

Is ProcalAmine PPN or TPN?

"ProcalAmine is a mixture of glycerol 3% and amino acid 3% that can be heat sterilized and supplied commercially. This product is used as PPN in some institutions."

Answered by AI

How is ProcalAmine administered?

"ProcalAmine was most commonly administered through central catheters 86% of the time, and through peripheral catheters only 14% of the time. Out of all the cases, the overall mechanical complication rate was 19%. Out of the 36 dogs, metabolic complications that could possibly be associated with ProcalAmine administration were found in 12 of them."

Answered by AI

Is ProcalAmine still available?

"The company has stopped making FreAmine III and ProcalAmine."

Answered by AI

Clinical Trials for Procalamine

Image of Rocky Mountain Kidney Care - Lone Tree in Lone Tree, United States.

AP301 for High Phosphate Levels

Any Age
All Sexes
Lone Tree, CO

The goal of this clinical trial is to learn if AP301 could work in the patients receiving maintenance dialysis with elevated blood phosphate. The main questions it aims to answer are: * Does AP301 lower blood phosphate levels? * Does AP301 works on serum calcium level, calcium times phosphate level, and intact parathyroid hormone level? * What discomfort or medical problem do the patients have when taking AP301? * Does AP301 improve quality of life in Chinese patients? The researchers will compare AP301 to an ineffective comparator (a look-alike substance that contains low dose AP301) to see if AP301 works to treat elevated blood phosphate. In the study, the patients will experience the following stages in a chronicle order: * Stop all using blood phosphate-lowering drugs, * Take AP301 or the comparator three times a day for 8 weeks, * Take AP301 three times a day for 24 weeks, and * Take AP301 or the comparator three times a day for 3 weeks. In the first 32 weeks, the dose of AP301 will be adjusted upwards or downwards based on the patient's blood phosphate level and the study doctor's judgment. If the participant has a blood phosphate level above or below a certain level, they may receive additional treatment to lower the blood phosphate level.

Phase 3
Recruiting

Rocky Mountain Kidney Care - Lone Tree (+18 Sites)

Alebund Pharmaceuticals