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BPaL(M) regimen

Asan Medical Center · FDA-approved active Small molecule

BPaL(M) regimen is a Anti-tuberculosis combination regimen Small molecule drug developed by Asan Medical Center. It is currently FDA-approved for Extensively drug-resistant tuberculosis (XDR-TB), Multidrug-resistant tuberculosis (MDR-TB). Also known as: Bedaquiline, Pretomanid, Linezolid, Moxifloxacin.

BPaL(M) is a combination regimen of bedaquiline, pretomanid, linezolid, and moxifloxacin that targets multiple pathways in Mycobacterium tuberculosis to overcome drug resistance.

BPaL(M) is a combination regimen of bedaquiline, pretomanid, linezolid, and moxifloxacin that targets multiple pathways in Mycobacterium tuberculosis to overcome drug resistance. Used for Extensively drug-resistant tuberculosis (XDR-TB), Multidrug-resistant tuberculosis (MDR-TB).

At a glance

Generic nameBPaL(M) regimen
Also known asBedaquiline, Pretomanid, Linezolid, Moxifloxacin
SponsorAsan Medical Center
Drug classAnti-tuberculosis combination regimen
TargetMultiple: ATP synthase (bedaquiline), cell wall synthesis (pretomanid), ribosomal protein synthesis (linezolid), DNA gyrase (moxifloxacin)
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhaseFDA-approved

Mechanism of action

The regimen combines four anti-tuberculosis agents with complementary mechanisms: bedaquiline inhibits ATP synthase, pretomanid is a prodrug activated by mycobacterial enzymes to disrupt cell wall synthesis, linezolid inhibits protein synthesis, and moxifloxacin inhibits DNA gyrase. This multi-target approach is designed to treat drug-resistant tuberculosis, particularly extensively drug-resistant (XDR-TB) and multidrug-resistant (MDR-TB) strains.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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Frequently asked questions about BPaL(M) regimen

What is BPaL(M) regimen?

BPaL(M) regimen is a Anti-tuberculosis combination regimen drug developed by Asan Medical Center, indicated for Extensively drug-resistant tuberculosis (XDR-TB), Multidrug-resistant tuberculosis (MDR-TB).

How does BPaL(M) regimen work?

BPaL(M) is a combination regimen of bedaquiline, pretomanid, linezolid, and moxifloxacin that targets multiple pathways in Mycobacterium tuberculosis to overcome drug resistance.

What is BPaL(M) regimen used for?

BPaL(M) regimen is indicated for Extensively drug-resistant tuberculosis (XDR-TB), Multidrug-resistant tuberculosis (MDR-TB).

Who makes BPaL(M) regimen?

BPaL(M) regimen is developed and marketed by Asan Medical Center (see full Asan Medical Center pipeline at /company/asan-medical-center).

Is BPaL(M) regimen also known as anything else?

BPaL(M) regimen is also known as Bedaquiline, Pretomanid, Linezolid, Moxifloxacin.

What drug class is BPaL(M) regimen in?

BPaL(M) regimen belongs to the Anti-tuberculosis combination regimen class. See all Anti-tuberculosis combination regimen drugs at /class/anti-tuberculosis-combination-regimen.

What development phase is BPaL(M) regimen in?

BPaL(M) regimen is FDA-approved (marketed).

What are the side effects of BPaL(M) regimen?

Common side effects of BPaL(M) regimen include Peripheral neuropathy, QT prolongation, Hepatotoxicity, Gastrointestinal disturbances, Anemia.

What does BPaL(M) regimen target?

BPaL(M) regimen targets Multiple: ATP synthase (bedaquiline), cell wall synthesis (pretomanid), ribosomal protein synthesis (linezolid), DNA gyrase (moxifloxacin) and is a Anti-tuberculosis combination regimen.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing