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Immutep and Lonza sign agreement for cell line selection, cell banking and process development of ImmuFact(R) IMP321

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Immutep and Lonza announced today an agreement for cell line selection, master cell banking and process development ofย ImmuFact(R) IMP321.

Lonza will initiate the process development for Immutepโ€™s lead product, using Immutep’s newly-developedย proprietary cell lines. Immutep announced Phase I/II results for IMP321 in an oral presentation at ASCO (American Society ofย Clinical Oncology conference) in 2010 describing its use in a chemo-immunotherapy protocol in first-line metastatic breastย cancer.

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โ€œWe are pleased to support Immutepโ€™s development initiatives,โ€ said Janet White, head of Lonza development services. โ€œThisย partnership directly reflects Lonzaโ€™s commitment to emerging biotechnology innovation through its clinical milestones.โ€

IMP321 (LAG-3Ig) has potential for the treatment of advanced cancer in combination with standard first-line chemotherapy.

IMP321 is an antigen presenting cell (APC) activator. Tumour-specific memory CD8 T cells are activated by these APC andย contribute to tumour regression.

โ€œWe have every confidence in Lonza to carry out the production for pivotal trials and beyond,โ€ said Dr. Frederic Triebel,ย scientific and medical director of Immutep. โ€œThe mechanism of action of this synergistic combination of chemotherapy andย active immunotherapy is very simple. The chemotherapy provides a burst of tumour cell debris and the surrounding APC take upย the tumour antigens. IMP321 activates these APC resulting in a long-lasting CD8 T cell response against the tumour. We thinkย that the combination of first-line standard chemotherapy plus IMP321 should be tested in several first-line indications. Weย are in partnering discussions at present.โ€

About ImmuFact(R) IMP321

IMP321 is an APC (antigen presenting cell) activator that has completed a Phase I/II clinical trial combined withย chemotherapy (chemo-immunotherapy) in first-line metastatic breast cancer. The trial showed that 90 per cent of the 30ย patients experienced clinical benefit at six months. In addition, the APC activation observed in the blood was dose-dependentย and correlated with the reduction of the tumour mass. IMP321 is a LAG-3Ig fusion protein produced in CHO (Chinese Hamsterย Ovary) cells.

AIPAC TRIAL

Immutep has started planning the AIPAC (Active Immunotherapy – PAClitaxel) Phase IIb/III clinical trial in first lineย metastatic breast cancer, following scientific advice from the EMA. Other trials in other cancers and with otherย chemotherapies will follow to expand the use of IMP321 in chemo-immunotherapy.

Chemoimmunotherapy

The objective of chemoimmunotherapy is to amplify natural pre-existing T cell responses specific for any known or unknownย tumour antigen and to recruit and amplify new tumour-specific T cell responses resulting from the use of cytotoxic drugs. Theย direct cytolytic effect of some cytotoxic drugs, such as paclitaxel, can enhance antigen loading of APC by inducing tumourย cell apoptosis.

Clinical Development History

More than 600 subcutaneous injections of IMP321 have been administered to date in Europe and the USA, at doses up to 30 mgย with no clinically significant drug-related adverse events. A Phase I trial in metastatic renal cell carcinoma with IMP321ย alone and a Phase I/II trial in metastatic breast cancer combining IMP321 with paclitaxel in a chemo-immunotherapy protocolย have been completed. Four Phase I/II clinical trials are in progress using IMP321 as adjuvant in cancer vaccines in:ย disease-free melanoma, metastatic melanoma treated by lympho-depletive/adoptive transfer, metastatic melanoma and prostateย cancer.

About Immutep S.A.

Immutep S.A. is a biopharmaceutical company developing immunostimulatory factors for the treatment of cancer andย immunomodulatory therapeutic antibodies for the treatment of cancer or autoimmune disease. The company’s technologies areย based on the LAG-3 immune control mechanism that mediates T cell immune responses. LAG-3 (CD223) is Lymphocyte-Activationย Gene-3. Apart from IMP321, described above, two of the Company’s other products are:- ImmuTune(R) IMP701

IMP701 is an antagonist anti-LAG-3 antibody. It gives rise to T cell proliferation in a similar manner to anti-CTLA-4 andย anti-PD-1 antibodies except that it also inhibits T regulatory cells (Tregs) giving it a unique double mode of action.

Partnering discussions are in progress.

– ImmuTune(R) IMP731

IMP731 is a depleting anti-LAG-3 antibody for autoimmune disease. This product is licensed to GSK.

For more information, visit http://www.immutep.com

About Lonza

Lonza is one of the world’s leading suppliers to the pharmaceutical, healthcare and life science industries. Products andย services span its customersโ€™ needs from research to final product manufacture. It is the global leader in the production andย support of active pharmaceutical ingredients both chemically as well as biotechnologically. Biopharmaceuticals are one of theย key growth drivers of the pharmaceutical and biotechnology industries. Lonza has strong capabilities in large and smallย molecules, peptides, amino acids and niche bioproducts, which play an important role in the development of novel medicinesย and healthcare products. Lonza is also the world leader in microbial control providing innovative, chemistry-based andย related solutions to destroy or to selectively inhibit the growth of harmful microorganisms. Its activities encompass theย areas of water treatment, personal care, health and hygiene, industrial preservation, materials protection and woodย treatment. In addition, Lonza is a leader in cell-based research, endotoxin detection and cell therapy manufacturing.

Furthermore, the company is a leading provider of value chemical and biotech ingredients to the nutrition and agro markets.

Lonza is headquartered in Basel, Switzerland and is listed on the SIX Swiss Exchange and secondary listed on the Singaporeย Exchange Securities Trading Limited (โ€œSGX-STโ€). Lonza is not subject to the SGX-STโ€™s continuing listing requirements. Lonzaย is subject to the listing rules of the SIX Swiss Exchange, which do not have specific requirements equivalent to the listingย rules of the SGX-ST in respect of interested person transactions, acquisition and realizations and delisting. In 2011, theย company had sales of CHF 2.69 billion.

Further information can be found at http://www.lonza.com

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