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HERCESSI (TRASTUZUMAB-STRF)

ACCORD BIOPHARMA INC. · FDA-approved approved ✓ Verified May 2026 Quality 6/100

HERCESSI (generic name: TRASTUZUMAB-STRF) is a drug developed by ACCORD BIOPHARMA INC.. It is currently FDA-approved.

Herceptin (ABP-980) is an antibody that inhibits the receptor protein-tyrosine kinase erbB-2, and it is being studied in clinical trials for various breast cancer conditions, including anatomic stages I, II, and IV, as well as metastatic and oligometastatic breast carcinoma.

At a glance

Generic nameTRASTUZUMAB-STRF
SponsorACCORD BIOPHARMA INC.
Therapeutic areaOther
PhaseFDA-approved

Approved indications

No approved indications tracked.

Common side effects

Serious adverse events

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 HERCESSI

What is HERCESSI?

HERCESSI (TRASTUZUMAB-STRF) is a pharmaceutical drug developed by ACCORD BIOPHARMA INC..

Who makes HERCESSI?

HERCESSI is developed and marketed by ACCORD BIOPHARMA INC. (see full ACCORD BIOPHARMA INC. pipeline at /company/accord-biopharma-inc).

What is the generic name of HERCESSI?

TRASTUZUMAB-STRF is the generic (nonproprietary) name of HERCESSI.

What development phase is HERCESSI in?

HERCESSI is FDA-approved (marketed).

What are the side effects of HERCESSI?

Common side effects of HERCESSI include Neutropenia, Fever, Nausea, Vomiting, Diarrhea, Fatigue. Serious adverse events: Cardiac failure, Hypersensitivity, Asymptomatic cardiac dysfunction, Interstitial pneumonitis.

Related

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