Last reviewed · How we verify

PF-06863135 + lenalidomide (pf-06863135-lenalidomide)

Pfizer · FDA-approved active ✓ Verified May 2026 Quality 45/100

PF-06863135 + lenalidomide (generic name: pf-06863135-lenalidomide) is a small molecule + immunomodulatory drug drug developed by Pfizer. It is currently FDA-approved for Relapsed or refractory multiple myeloma in combination with dexamethasone, Relapsed or refractory multiple myeloma in combination with dexamethasone and daratumumab, Relapsed or refractory multiple myeloma in combination with dexamethasone and daratumumab and carfilzomib.

PF-06863135 (elranatamab) is being studied in combination with lenalidomide for the treatment of multiple myeloma, including newly diagnosed multiple myeloma that is transplant ineligible. The combination of elranatamab and lenalidomide is being investigated in a clinical trial (NCT05623020) sponsored by Pfizer.

At a glance

Generic namepf-06863135-lenalidomide
SponsorPfizer
Drug classsmall molecule + immunomodulatory drug
Targetunknown
Therapeutic areaOncology
PhaseFDA-approved
Annual revenue2951

Approved indications

Common side effects

No common side effects on file.

Drug interactions

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
SEC EDGARRevenue + earnings

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 PF-06863135 + lenalidomide

What is PF-06863135 + lenalidomide?

PF-06863135 + lenalidomide (pf-06863135-lenalidomide) is a small molecule + immunomodulatory drug drug developed by Pfizer, indicated for Relapsed or refractory multiple myeloma in combination with dexamethasone, Relapsed or refractory multiple myeloma in combination with dexamethasone and daratumumab, Relapsed or refractory multiple myeloma in combination with dexamethasone and daratumumab and carfilzomib.

What is PF-06863135 + lenalidomide used for?

PF-06863135 + lenalidomide is indicated for Relapsed or refractory multiple myeloma in combination with dexamethasone, Relapsed or refractory multiple myeloma in combination with dexamethasone and daratumumab, Relapsed or refractory multiple myeloma in combination with dexamethasone and daratumumab and carfilzomib, Relapsed or refractory multiple myeloma in combination with dexamethasone and daratumumab and carfilzomib and isatuximab, Relapsed or refractory multiple myeloma in combination with dexamethasone and daratumumab and carfilzomib and isatuximab and elotuzumab.

Who makes PF-06863135 + lenalidomide?

PF-06863135 + lenalidomide is developed and marketed by Pfizer (see full Pfizer pipeline at /company/pfizer).

What is the generic name of PF-06863135 + lenalidomide?

pf-06863135-lenalidomide is the generic (nonproprietary) name of PF-06863135 + lenalidomide.

What drug class is PF-06863135 + lenalidomide in?

PF-06863135 + lenalidomide belongs to the small molecule + immunomodulatory drug class. See all small molecule + immunomodulatory drug drugs at /class/small-molecule-immunomodulatory-drug.

What development phase is PF-06863135 + lenalidomide in?

PF-06863135 + lenalidomide is FDA-approved (marketed).

What is PF-06863135 + lenalidomide's annual revenue?

PF-06863135 + lenalidomide generated approximately $0.0B in annual revenue.

What does PF-06863135 + lenalidomide target?

PF-06863135 + lenalidomide targets unknown and is a small molecule + immunomodulatory drug.

Related

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