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Part A

GlaxoSmithKline · FDA-approved active Small molecule Quality 5/100

Part A is a Small molecule drug developed by GlaxoSmithKline. It is currently FDA-approved. Also known as: KETAMINE GROUP, Rituximab, Doxil, pegylated liposomal doxorubicin.

Part A, marketed by GlaxoSmithKline, holds a significant position in its therapeutic area with a key composition patent expiring in 2028. The drug's primary strength lies in its established market presence and revenue generation. The primary risk is the potential increase in competition following the patent expiry in 2028.

At a glance

Generic namePart A
Also known asKETAMINE GROUP, Rituximab, Doxil, pegylated liposomal doxorubicin, cyclophosphamide
SponsorGlaxoSmithKline
ModalitySmall molecule
PhaseFDA-approved

Approved indications

No approved indications tracked.

Common side effects

No common side effects on file.

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

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:

Frequently asked questions about Part A

What is Part A?

Part A is a Small molecule drug developed by GlaxoSmithKline.

Who makes Part A?

Part A is developed and marketed by GlaxoSmithKline (see full GlaxoSmithKline pipeline at /company/gsk).

Is Part A also known as anything else?

Part A is also known as KETAMINE GROUP, Rituximab, Doxil, pegylated liposomal doxorubicin, cyclophosphamide.

What development phase is Part A in?

Part A is FDA-approved (marketed).

Related

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