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Who Makes Vectibix? The Manufacturer Behind This Targeted Cancer Therapy

2 min read

Originally developed by Abgenix Inc., Vectibix (panitumumab) has been manufactured and commercialized by the biopharmaceutical company Amgen Inc. since it acquired Abgenix in 2006. This acquisition gave Amgen full ownership and control over the drug, solidifying its role in bringing this important metastatic colorectal cancer treatment to market.

Quick Summary

Amgen Inc. is the manufacturer of Vectibix, a fully human monoclonal antibody for treating metastatic colorectal cancer. The drug originated with Abgenix and was integrated into Amgen's portfolio following its acquisition of Abgenix in 2006.

Key Points

  • Manufacturer: Vectibix (panitumumab) is manufactured and marketed by the global biopharmaceutical company Amgen Inc..

  • Origin: The drug was originally developed by Abgenix Inc., which Amgen acquired in 2006, thereby securing ownership.

  • Mechanism: As a fully human monoclonal antibody, Vectibix inhibits the epidermal growth factor receptor (EGFR) to block cancer cell growth signals.

  • Targeted Therapy: Vectibix is indicated for patients with wild-type RAS metastatic colorectal cancer, requiring a diagnostic test to confirm mutation status.

  • Biotechnology: The manufacturing process involves genetically engineered Chinese Hamster Ovary (CHO) cells to produce the panitumumab protein.

  • Global Reach: Amgen leverages international partnerships with companies like Zhejiang Beta Pharma and Takeda to distribute and commercialize Vectibix worldwide.

  • Milestones: Key milestones include initial 2006 FDA approval and a more recent 2025 approval for a combination therapy targeting specific KRAS mutations.

In This Article

Amgen Inc.: The Manufacturer of Vectibix

Amgen Inc., a global biopharmaceutical company based in Thousand Oaks, California, is the manufacturer responsible for the production and distribution of Vectibix (panitumumab). Amgen is a leader in biotechnology, developing innovative human therapeutics for serious illnesses. Vectibix, a targeted therapy for specific types of metastatic colorectal cancer (mCRC), is a significant part of Amgen's oncology portfolio. Amgen not only manufactures the drug but also conducts clinical trials to explore new uses, such as its recent approval in combination with Lumakras for KRAS G12C-mutated mCRC.

The Journey of Vectibix: From Abgenix to Amgen

The development of Vectibix began with Abgenix Inc. and its XenoMouse platform technology, which was used to create the fully human monoclonal antibody, panitumumab. This technology uses genetically engineered mice to produce antibodies with human composition, reducing the likelihood of immune reactions. In 2006, Amgen acquired Abgenix, gaining complete ownership of panitumumab and the rights to its development and commercialization. This acquisition was crucial for Amgen to advance the drug through clinical trials and obtain regulatory approvals, including the initial FDA approval in 2006.

Understanding Vectibix and Its Mechanism of Action

Vectibix is a targeted therapy that inhibits the epidermal growth factor receptor (EGFR). Panitumumab, the active ingredient, is a monoclonal antibody that binds to EGFR, a protein on cell surfaces involved in growth and multiplication. EGFR is often over-expressed in colorectal cancer, promoting uncontrolled cell growth. By blocking EGFR, Vectibix disrupts these growth signals. It is effective in patients with wild-type RAS mCRC; mutations in KRAS and NRAS genes can affect the drug's efficacy. {Link: FDA Approves Vectibix® (Panitumumab) For Use In Wild-Type RAS ... https://www.amgen.com/newsroom/press-releases/2017/06/fda-approves-vectibix-panitumumab-for-use-in-wildtype-ras-metastatic-colorectal-cancer}

Comparing Vectibix with another EGFR inhibitor

Vectibix is compared to cetuximab (Erbitux), another anti-EGFR therapy.

Feature Vectibix (Panitumumab) Cetuximab (Erbitux)
Manufacturer Amgen Inc. ImClone LLC (owned by Eli Lilly)
Antibody Type Fully human Chimeric (part mouse, part human)
Immune Response Risk Lower due to fully human nature Higher due to chimeric nature
Primary Indication Wild-type RAS mCRC Wild-type RAS mCRC and head and neck cancer
Companion Diagnostics Requires RAS mutation test Requires RAS mutation test

Conclusion: A Legacy of Innovation

Amgen is the manufacturer of Vectibix, a targeted therapy for metastatic colorectal cancer. The drug's development originated with Abgenix's innovative technology, and Amgen's acquisition of Abgenix in 2006 solidified its role in manufacturing and advancing the drug. Amgen's ongoing research and global partnerships have expanded the availability and potential uses of Vectibix, reflecting the company's commitment to developing advanced treatments. {Link: Amgen® SupportPlus | Vectibix® (panitumumab) https://www.vectibix.com/resources-amgen-supportplus}

Frequently Asked Questions

Vectibix (panitumumab) is manufactured and commercialized by the biopharmaceutical company Amgen Inc..

The active ingredient, panitumumab, was originally developed by Abgenix Inc. using its XenoMouse platform technology. Amgen later acquired Abgenix in 2006.

Vectibix is the brand name for panitumumab. While it may be distributed through partner companies in various countries, the manufacturing and brand are controlled by Amgen.

Yes, Amgen is heavily involved in oncology and produces a broad portfolio of innovative medicines for treating various types of cancer.

Vectibix is a biologic drug produced using recombinant DNA technology in genetically engineered mammalian cells, specifically Chinese Hamster Ovary (CHO) cells.

Yes, the rights to panitumumab, and subsequently the manufacturing of Vectibix, transferred to Amgen Inc. after it acquired the original developer, Abgenix Inc., in 2006.

Yes, Amgen has established partnerships and joint ventures to expand the commercialization of Vectibix in international markets, including with Zhejiang Beta Pharma in China and Takeda in Japan.

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Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.