Plus Therapeutics

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Plus Therapeutics
Nasdaq: PSTV
Headquarters
United States Edit this on Wikidata

Plus Therapeutics, Inc. is a clinical-stage pharmaceutical company developing innovative, targeted radiotherapeutics for adults and children with rare and difficult-to-treat cancers. The company is headquartered in Austin, Texas, United States.[1]

Company history[edit]

Plus Therapeutics, Inc. was formerly known as Cytori Therapeutics, Inc. In 2017, Cytori Therapeutics announced that it had acquired a nanomedicine platform.[2] In 2019, Cytori Therapeutics announced that it had divested its autologous cell therapy assets to Lorem Vascular of Australia and Seijiro Shirahama of Japan.[3] In 2019, Cytori Therapeutics announced that it had changed its focus and name to Plus Therapeutics.[4] In 2020, Plus Therapeutics announced that it had licensed a novel oncology platform, including multiple radiopharmaceutical assets.

Core technology: Rhenium NanoLiposome radiotherapeutics[edit]

Plus Therapeutics is developing nanoliposome-encapsulated BMEDA-chelated radioisotope drugs to treat various types of cancer. Rhenium (186Re) Obisbemeda is a Rhenium-186 radiolabeled therapeutic targeting recurrent glioblastoma, leptomeningeal metastases, and pediatric brain cancers. Their BMEDA loading technology coupled with Rhenium-186 allows for the entrapment the radiation particle within a nanoliposome carrier, facilitating accumulation and retention in the tumor tissue. This approach supports higher, more effective radiation doses without significant toxicity.[5]

Rhenium-186 (186Re) (half-life 90 hours) is a reactor produced isotope with great potential for medical therapy. It is in the same chemical family as Technetium-99m (99mTc), a radioactive tracer that is the most commonly used isotope for diagnostic scintigraphic imaging in nuclear medicine. Like 99mTc, rhenium is not taken up by bone and is readily cleared by the kidneys.

While 186Re emits therapeutic beta particles, every 10th isotope decay also produces a gamma photon. The average 186Re beta particle path length in tissue of 2 millimeters is ideal for treatment of solid tumors. Additionally, the emitted gamma photons have similar photon energy to those emitted by 99mTc, allowing for imaging of the isotope within the body on standard nuclear imaging equipment available in routine medical practice. Therefore, the 186Re isotope has great potential in Convection Enhanced Delivery (CED) applications of local therapy of solid tumors. However, a carrier is needed to deliver the isotope to the brain and maintain its localization at the desired site, as otherwise it would quickly disperse and be carried away from the site of injection by the circulatory system.

Nanotechnology describes the use of atoms, molecules, or compounds to create extremely small materials and structures, having a size of 100 to 1 nanometers, with special properties that can be applied across many disciplines including electronics, energy, environment, and medicine. In medicine, these materials and structures are often used for site-specific drug delivery and take the form various organic and inorganic nanoparticles. Nanoparticle morphology, both size and shape, affects how cells in the body “see” these nanoparticles and ultimately influences their toxicity, distribution, and targeting ability. Of the various nanotechnology drug delivery systems, NanoLiposomes have been extensively explored and undergone significant technical advances since they were first developed in 1965. Today, many are regulatory-approved and clinically- and commercially-proven across multiple medical areas including, but not limited to, cancer treatment, fungal infections, and pain management. NanoLiposomes are small, complex, spontaneously-forming drug carriers consisting of a precise formulation of naturally occurring phospholipids and cholesterol — nearly identical to the lipid membranes of normal human cells. This means that there are natural degradation pathways in the human body for these lipid nanoparticles. NanoLiposome properties such as size and structure, electrical charge, lipid composition, and surface modification are each critical to the ability of the product to provide reproducible drug delivery required by regulatory authorities and relied upon by physicians and patients. Although larger liposomes can be manufactured, the most useful size range for drug carrier applications is 80-100 nanometers. NanoLiposomes of this size have the ability to facilitate retention at the site of injection.

NanoLiposomes in the 100 nanometer size range have been the most investigated carrier for convection-enhanced delivery (CED) of drugs to the brain. These studies include the use of CED-delivery of NanoLiposomes carrying chemotherapeutic agents directly to brain tumor, including drugs such as irinotecan and topotecan. If NanoLiposomes are to be utilized as a carrier for radioisotopes, a method for the efficient loading of NanoLiposomes with the radioisotopes is needed. Such a method has been developed for the labeling of NanoLiposomes with radiotherapeutic Rhenium radionuclides to very high levels of specific activity. This novel approach uses a specially developed molecule known as BMEDA-2 to chelate with Rhenium-186 and carry it into the interior of a NanoLiposome where it is irreversibly trapped.

ReSPECT-GBM Clinical Trial for Recurrent Glioblastoma[6][edit]

The purpose of the ReSPECT-GBM Clinical Trial is to assess the safety, tolerability, and distribution of a new medication, Rhenium (186Re) Obisbemeda, in adults with recurrent glioblastoma after standard surgical, radiation, and/or chemotherapy treatment. ReSPECT-GBM is supported by the U.S. National Institutes of Health / National Cancer Institute and has a National Trial Number of NCT01906385. As of January 2024, the study is enrolling Phase 2 patients and has clinical study site locations at UT Health San Antonio in San Antonio, Texas, UT Southwestern Medical Center in Dallas, Texas, and UT MD Anderson Cancer Center in Houston, Texas. [7][8][9]

According to the most recent CBTRUS Statistical Report,[10] annually there are approximately 12,900 cases of glioblastoma diagnosed, with historical 1 year and 5 year relative survival rates of 40.8% and 6.8%, respectively. The poor survival is attributable partly to the nature of the tumor. The infiltrative nature of glioblastoma results in difficulty eliminating microscopic disease despite macroscopic gross-total resection, with 90% of patients having recurrence at the original tumor location. The location of the tumor also makes drug delivery difficult with only small or lipophilic molecules able to cross the blood brain barrier to reach the tumor. Of those agents that are able to reach the tumor, glioblastomas have shown to be resistant to most cytotoxic agents and to quickly develop resistance when initially sensitive.

ReSPECT-LM Clinical Trial for Leptomeningeal Metastases[11][edit]

Plus Therapeutics is developing Rhenium (186Re) Obisbemeda, an innovative, targeted radiotherapeutic for multiple rare and difficult-to-treat cancers including Leptomeningeal Metastases (LM). In the U.S. multi-center ReSPECT-LM Phase 1 clinical trial, Rhenium (186Re) Obisbemeda will be administered through an intraventricular catheter (Ommaya reservoir) in patients with LM. The treatment consists of a single administered dose of 186RNL per patient on an outpatient basis by the clinical trial physician. The ReSPECT-LM U.S. Phase 1 Clinical Trial is enrolling patients as of January 2024 and has clinical study site locations at UT Health San Antonio in San Antonio, Texas, UT Southwestern Medical Center in Dallas, Texas, and Northwestern Memorial Hospital in Chicago, Illinois. [12]

The ReSPECT-LM clinical trial is funded, in part, by a $17.6 million grant from the Cancer Prevention & Research Institute of Texas, the second largest public funding source for cancer research in the world. The National Trial Number for this clinical trial is NCT05034497.[13]

Leptomeningeal metastases (LM) are a rare but typically fatal complication of advanced cancer in which cancer cells spread to the central nervous system (CNS) and are found in either the leptomeninges (membrane surrounding the brain and spinal cord) or cerebrospinal fluid (CSF) (circulates nutrients and chemicals to the brain and spinal cord). Leptomeningeal Metastases is sometimes referred to as leptomeningeal cancer, leptomeningeal disease, neoplastic meningitis, or meningeal carcinomatosis, and is most commonly found in patients with melanoma, breast, lung, or gastrointestinal cancer. Despite affecting over 110,000 people annually in the U.S., there are currently no FDA approved treatments specifically for Leptomeningeal Metastases.[14]

ReSPECT-PBC Clinical Trial for Pediatric Brain Cancer[15][edit]

Plus Therapeutics is developing the Rhenium (186Re) Obisbemeda radiotherapeutic for the treatment of rare, frequently fast-growing pediatric brain and spinal cord tumors with a poor prognosis – diffuse instrinsic pontine glioma (DIPG), ependymoma and high-grade glioma (HGG). The ReSPECT-PBC (Pediatric Brain Cancer) U.S. Phase 1 Clinical Trial is planned to initiate in 2024.[16]

Cancer is the leading cause of death by disease among children in the U.S. Brain and spinal cord tumors are the 2nd most common cancers in children, accounting for ~26% of childhood cancers.

DIPG is a rare, fast-growing CNS tumor that forms in glial cells in the pons region of the brain stem; spreads to nearby tissue and other parts of the brain stem, are hard to treat, and have a poor prognosis.[17]

Ependymoma is a rare, slow- or fast-growing (depends on Grade) primary CNS tumor that forms in ependymal cells that line the ventricles of the brain and the center of the spinal cord; may spread throughout the CNS but spread outside of the CNS is rare; all can recur but often patients are tumor-free for years before testing shows new tumor growth, either at the same location as the first tumor or somewhere else within the CNS.[18][19]

HGG is a rare, fast-growing CNS tumor that forms in glial cells of the brain and spinal cord; can be found almost anywhere within the CNS, but are most commonly within the supratentorium in children ages 15–19; HGG found in children are different from those in adults.[20]

Other research and applications[edit]

Rhenium is a versatile radioisotope (radioactive isotope) that emits beta energy with a short half-life (17 to 90 hours) and sufficient energy for destroying tumor tissue – as well as a gamma energy with photons for live imaging through the treatment process. Plus Therapeutics leverages two different radioisotopes, Rhenium-186 and Rhenium-188, which offer unique physical properties for treating various tumor sizes and types. Rhenium-186 is nuclear reactor-produced 1.8 mm average radiation path length of beta energy and suitable for treating small and medium size tumors. Rhenium-188 is generator-produced for quick availability 3.1 mm average radiation path length of beta energy and suitable for treating large size tumors.[21]

As of January 2024, the company is evaluating the safety and efficacy of 188RNL-BAM in preclinical trials for targeting primary liver cancer, hepatocellular carcinoma, and secondary liver cancer, metastatic colorectal cancer.[22]

References[edit]

  1. ^ "Home - Plus Therapeutics (PSTV)". Plus Therapeutics. Retrieved 29 May 2022.
  2. ^ "Cytori to Acquire Proprietary Nanoparticle Development". Globenewswire.com. Retrieved 29 May 2022.
  3. ^ "Japan Cell Therapy Transaction Yields $3MM". Globenewswire.com. Retrieved 29 May 2022.
  4. ^ "Plus Therapeutics, Inc. Announces Nasdaq Ticker Symbol Changes and Reverse Stock Split" (Press release). GlobeNewswire. 29 July 2019.
  5. ^ "Pipeline - Plus Therapeutics (PSTV)". plustherapeutics.com. 2 December 2021. Retrieved 23 January 2024.
  6. ^ "Recurrent Glioblastoma (GBM)". ReSPECT™ Clinical Trials. Retrieved 23 January 2024.
  7. ^ "Recurrent Glioblastoma - ReSPECT™ Clinical Trials". Respect-trials.com. Retrieved 29 May 2022.
  8. ^ "Maximum Tolerated Dose, Safety, and Efficacy of Rhenium Nanoliposomes in Recurrent Glioma (ReSPECT) - Full Text View". ClinicalTrials.gov. Retrieved 29 May 2022.
  9. ^ "U.S. ReSPECT Clinical Trial | Rhenium NanoLiposome (RNL™) | Recurrent Glioblastoma". ReSPECT™ Clinical Trials. Retrieved 23 January 2024.
  10. ^ "CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2012–2016". Academic.oup.com. doi:10.1093/neuonc/noz150. Retrieved 29 May 2022.
  11. ^ "Leptomeningeal Metastases (LM) - ReSPECT Clinical Trials". ReSPECT™ Clinical Trials. Retrieved 23 January 2024.
  12. ^ "Leptomeningeal Metastases (LM) - ReSPECT Clinical Trials". ReSPECT™ Clinical Trials. Retrieved 23 January 2024.
  13. ^ "Leptomeningeal Metastases - ReSPECT™ Clinical Trials". Respect-trials.com. Retrieved 29 May 2022.
  14. ^ "U.S. ReSPECT Clinical Trial | Rhenium NanoLiposome (RNL™) | Recurrent Glioblastoma". ReSPECT™ Clinical Trials. Retrieved 23 January 2024.
  15. ^ "U.S. ReSPECT Clinical Trial | Rhenium NanoLiposome (RNL™) | Recurrent Glioblastoma". ReSPECT™ Clinical Trials. Retrieved 23 January 2024.
  16. ^ "Pediatric Brain Cancer - ReSPECT™ Clinical Trials". Respect-trials.com. Retrieved 29 May 2022.
  17. ^ Mosier, Jenny (28 December 2020). "What is DIPG? - Michael Mosier Defeat DIPG Foundation". Defeatdipg.org. Retrieved 29 May 2022.
  18. ^ Amy F. (10 May 2022). "Ependymoma Cancer Research Network". CERN Foundation. Retrieved 29 May 2022.
  19. ^ "U.S. ReSPECT Clinical Trial | Rhenium NanoLiposome (RNL™) | Recurrent Glioblastoma". ReSPECT™ Clinical Trials. Retrieved 23 January 2024.
  20. ^ "U.S. ReSPECT Clinical Trial | Rhenium NanoLiposome (RNL™) | Recurrent Glioblastoma". ReSPECT™ Clinical Trials. Retrieved 23 January 2024.
  21. ^ "Our Platform - Plus Therapeutics (PSTV)". plustherapeutics.com. 5 December 2021. Retrieved 23 January 2024.
  22. ^ "Pipeline - Plus Therapeutics (PSTV)". plustherapeutics.com. 2 December 2021. Retrieved 23 January 2024.

External links[edit]

  • Official website
  • Clinical Trial Website
  • Business data for Plus Terapeutics, Inc.:
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