Advanced Accelerator Applications

Advanced Accelerator Applications (AAA or Adacap) is a France-based pharmaceutical group, specialized in the field of nuclear medicine.PrivateEquityWire, "Advanced Accelerator Applications completes fundraising", Feb 18th, 2014
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The group operates in all three segments of nuclear medicine ( PET, SPECT and therapy) to diagnose and treat serious conditions in the fields of oncology, neurology, cardiology, infectious and inflammatory diseases.Il Sole 24 Ore, "Dal Cern and Biopark canavese", March 12th, 2014
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In late October 2017, ''Reuters'' announced that Novartis would acquire the company for $3.9 billion, paying $41 per ordinary share and $82 per American depositary share representing a 47 percent premium. On January 22, 2018, Novartis AG announced the successful completion of the tender offer by its subsidiary, Novartis Groupe France S.A.

History

AAA was created in 2002 by Italian physicist Stefano Buono to exploit a patent from the European Organization for Nuclear Research ( CERN).AdnKronos," Research: from Rubbia to AAA, great success for an Italian physicist with European company"
March 19th, 2010.

AAA currently has a total of 31 sites in 12 countries, including: 19 production facilities in 8 countries (in Europe and the U.S.) that manufacture targeted radioligand therapies and precision imaging radioligands, and 6 sites with R&D activity.

In October 2017, Novartis announced that it intended to acquire the company for US$3.9 billion.

Products

AAA has a portfolio of diagnostic and therapeutic applications and products in the fields of Molecular Imaging and Therapy.

The group's portfolio of radiopharmaceuticals includes radioactive agents for positron emission tomography ( PET) imaging as well as single-photon emission computed tomography ( SPECT) diagnostic products.

Lutathera

The company's lead product is LUTATHERA, a Lutetium Lu 177 dotatate labeled somatostatin analogue peptide, a theragnostic cancer product being developed to treat certain gastro-entero pancreatic neuroendocrine tumors ( GEP-NETs). It selectively targets over-expressed somatostatin receptors while also giving off gamma emissions to allow physicians to visualize where in the body both the drug and the tumor are.
It was approved by the FDA in January 2018 for GEP-NET.

Approval

Lutathera, also known as lutetium Lu 177 dotatate, is a target treatment drug for patients with GEP-NETs. Its approval for Advanced Accelerator Applications was announced on January 26, 2018, by the US Food and Drug Administration. Lutathera is most notable as the first FDA approved peptide receptor radionuclide therapy (PRRT) to combat GEP-NETs.

= GEP-NETs

=
GEP-NETs are rare groups of cancer that continue to proliferate, regardless of initial therapy treatments. They are present in areas affected by pancreatic or gastrointestinal cancers; specifically, the pancreas, stomach, intestines, colon and rectum.

Use

Lutathera is used to combat pancreatic and gastrointestinal cancers that do not respond well to common chemotherapeutical treatments; namely for patients with somatostatin receptor-positive GEP-NETs. These receptors are commonly found on tumors located in the foregut, midgut, and hindgut.

Mechanism

Lutathera is a radioactive drug consisting of a tyrosine-containing somatostatin analog Tyr3-octreotate (TATE) attached to the chelating agent tetraazacyclododecanetetra-acetic acid (DOTA). Attached to the dotatate is the radioactive marker Lu-177, a radioisotope. The dotatate binds to the GEP-NET positive somatostatin receptor cells commonly present on neuroendocrine tumors. After binding to the receptor, Lutathera enters the cell and uses its radioactive property to damage DNA. This mechanism effectively triggers apoptosis of cancerous tumor cells. As a result, studies found that 16% of patients being treated with Lutathera experienced either complete or partial tumor shrinkage.

Studies

FDA approval of Lutathera was ultimately supported by two clinical studies. NETTER-1, a Phase 3 study, was a randomized clinical trial which included patients with a severe form of somatostatin receptor-positive NETs. The study compared Lutathera treatment with a standard dose of octreotided LAR against a high-dose of octreotide LAR. Researchers measured tumor growth after the course of the treatment, also known as progression-free survival. The study concluded that patients who were treated with Lutathera lived substantially longer compared to those who only received the octreotide treatment. They experienced a 79% reduction in death and cancer progression.

The Netherlands study gathered several patients with somatostatin receptor-positive tumors, including patients with GEP-NETs. The study found that 16% of patients with GEP-NETs, who were treated with Lutathera, experienced complete or partial tumor shrinkage. As a result, a pre-planned interim overall survival analysis found that Lutathera treatment lead to a 48% reduction in risk of death.

Common Grade 3-4 Adverse Reactions

Advances

Lutathera is a major technological advancement for the detection of tumors. Diagnostic imaging that relies on dotatates can now rely on Lutathera to locate somatostatin receptor-positive tumors by tagging them with its radioactive component. This tagging of tumors will allow them to become more visible during positron emission tomography (PET) scans. With LU-177 dotatates, more somatostatin receptor-positive GEP-NET patients can be identified for treatment of the disease.

Pipeline

AAA has a broad pipeline of products in development, including several theragnostic pairings for oncology indications.

NETSPOT and SomaKit TOC are novel kits for radiolabeling somatostatin analogue peptides to help diagnose somatostatin receptor-positive NET lesions. Each kit has received orphan drug designation from both the EMA and the FDA.Devicespace.com, "Advanced Accelerator Applications Receives Orphan Drug Designation From FDA And European Medicines Agency For Gallium-68 DOTATATE For Use In Patients With Gastro-Entero-Pancreatic Neuroendocrine Tumors"
. 3 March 2014.News Medical, "AAA gets orphan drug designation status for radiopharmaceutical, Gallium-68 DOTATATE"
4 March 2014.

99MTc-rhAnnexin V-128, a SPECT investigational candidate for the diagnosis and assessment of apoptotic and necrotic processes, which are present in a number of pathological conditions in oncology and cardiovascular disease, as well as in autoimmune disorders. 99MTc-rhAnnexin V-128 is currently in a Phase I/II trial for the diagnosis of rheumatoid arthritis and ankylosing spondylitis, as well as several Phase II studies in cardiovascular, cardio-oncology, and pulmonary indications.

¹⁷⁷Lu-PSMA-617 and ⁶⁸Ga-PSMA-617 are in development to treat, image, monitor and stage prostate cancer. PSMA-617 is a ligand of prostate-specific membrane antigen (PSMA) expressed on the majority of prostate tumor cells. ¹⁷⁷Lu-PSMA-617 also known as lutetium (¹⁷⁷Lu) vipivotide tetraxetan is being developed to treat prostate cancer by binding to PSMA-617. In June 2021 it was granted a breakthrough therapy designation. ⁶⁸Ga-PSMA-617 is under development as a complementary diagnostic candidate.

CTT1057 is an 18F-labeled investigational diagnostic candidate in development for PET imaging of prostate cancer. CTT1057 is a phosphoramidate-based peptide, which specifically binds to Prostate-Specific Membrane Antigen (PSMA), expressed on the majority of prostate tumor cells.

177LuNeoBOMB1 and 68GaNeoBOMB1 are new generation antagonist bombesin analogs in development to treat, image, monitor and stage gastrin-releasing peptide receptor (GRPR)-expressing malignancies, such as such as gastrointestinal stromal tumors (GIST), prostate cancer and breast cancer. 177LuNeoBOMB1 is a therapeutic candidate and 68GaNeoBOMB1 is its complementary diagnostic candidate.

Millburn site

In 2016, AAA opened a light manufacturing and distribution site in Millburn, NJ, a residential town in North Jersey.Danielle Desisto
"Millburn manufacturing site safely produces cancer-fighting drug"
When the site was first purchased, it caused substantial concerns among local residents."Concerns raised about proposed cancer drug factory in Millburn"
/ref> Per the requests of Millburn Residents, the Township Committee hired a nuclear/radiology expert to re-assess the appropriateness of opening a radioactive manufacturing site in the residential area.Cecilia Levine
"Nuclear meds expert hired"
''The Record''. 7 May 2015. The expert concluded that the proposed operations at AAA are safe and pose no hazard to the citizens of Millburn.Jonathan Sym
"Advanced Accelerator Application Investigation Results: Risks Are "Close To Zero Without Being Zero" Says Expert". ''Tap Into Millburn/Short Hills''. 18 February 2016.
/ref>Harry Trumbore
"Expert says radiopharmaceutical factory proposed for Millburn is safe"
. 11 February 2016

References

External links

* {{Official website, www.adacap.com

Pharmaceutical companies of France
French companies established in 2002
Pharmaceutical companies established in 2002
Companies based in Auvergne-Rhône-Alpes