Accelerated Evolution Biotechnologies AEBI Ltd Israel

AEBi was established in the year 2000, and has been managed since then based on the idea that the ability to manipulate and design peptides has vastly superior advantages to many, if not any, existing and trajectory technologies of drug development. This idea is valid today as well.The basic idea is that we do not require a natural lead or a sequence (usually coming from the academia or other research) which are either not strong enough or not specific enough and difficult to manipulate in order to create a drug.
An artificial high complexity pool, representing a broad spectrum of  possibilities, manipulated by our technology, will provide the best possible solution. Such a  solution  will not be hindered or blocked by natural interactions and will be very specific to the problem.
AEBi, a development-stage biopharmaceutical company engaged in discovery and development of therapeutic peptides, has developed a combinatorial biology screening platform technology (IP protected).
The major advantage is that it can be used not only to find binders to known targets, but to select the best functional molecules among them. AEBi's platform is very flexible, exploiting combinatorial biology to discover new and better lead compounds to disease targets.

Our Breakthrough SoAP Platform:
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Our platform provides functional leads to very difficult targets (functional leads - agonist, antagonist, inhibitor, etc.), not merely those that best bind with the target.

Moreover, it allows us to develop drugs to many illnesses, among them CANCER and COVID19, and is expected to transform the drug discovery R&D phase by significantly reducing the attrition rate of new drug candidates.
This Breakthrough technology generates very specific lead compounds with greater functionality and improved pharmacological properties. Such lead Compounds will allow more effective drugs and fewer side effects. The need for such technology is acute and pressing for many reasons. The sole external requirement in the screening process is a Defined Target (usually an illness-related protein).

MuTaTo: our Multiple Targeted Comprehensive Cancer Therapy
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This new cancer treatment is a personalized medicine concept, that can be also turned into a "shelf product". The main principal of it is using multiple targeting peptides connected together with a toxin. The main advantage of it is that it would lower the probability of the targeted cancer cells to develop drug-resistance due to mutations they possess, and at the same time would lower adverse effects due to avidity effect. Each cancer patient would receive a specific drug perfectly suited to his/her cancer, based on the expression profile of receptors on the outer membrane of their cancer cells. This therapy's construct production is easy and rapid. Therefore, the production cost would not be as expensive as with other biological drugs, or other sophisticated cancer treatments.
MuTaTo our Multiple Targeted Safe Cancer Therapy is DIFFERENT and UNIQUE because:
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1- It is EFFECTIVE on almost all types of CANCERS because we will develop a MuTaTo molecule for every type of cancers.
2- it is SAFE on healthy cells and DOESN'T cause any suffering to patients.
3- unlike other cancer therapies that attack cancer from only one or 2 targets at most , MuTaTo is DIFFERENT because it attacks cancer from at least 3 targets so that cancer DOESN'T metastasize nor develop drug resistance.
4- MuTaTo can treat almost all types of cancers even rare one and is effective on all cancer stages even terminal ones.
5- our MuTaTo is so versatile it can be:
a) used as personalized Cancer therapy where each cancer patient would receive a specific drug perfectly suited to his/her cancer, based on the expression profile of receptors on the outer membrane of their cancer cells.
b) or it can be mass produced as a "shelf Product - Oncolytic Drug" to treat different cancers with different indications, so we will have not just one MuTaTo Drug, but a COMPLETE FAMILY OF MuTaTo DRUGS, to treat almost all types and indications of Cancers , from all stages, even rare and Terminal cancers.

Our MUTATO Cancer treatment is PATENTED,
https://patents.google.com/patent/WO2018061004A1/en?inventor=Ilan+morad&oq=Ilan+morad

Our PLATFORM is patented
https://patents.google.com/patent/WO2007010525A3/en?inventor=Ilan+morad&oq=Ilan+morad

Our concept is peer approved and we have proof of concept, and published in the prestigious Cancer Therapy Magazine
https://m.scirp.org/papers/98400

-Chinese Journals have written about our concept including MyBioGate
https://mp.weixin.qq.com/s/NYjbJDgdBOtxsAztKr7wMw
独家回访 | 一年内彻底治愈癌症,炒作还是事实?
徐子宜 Ginger 美柏企业服务
here is one article about us in another journal:
https://www.myzaker.com/article/5f88ec9f32ce40ea2900000a
Website:
www.aebi-bio.com
Company Size (Fulltime employees)
Year of foundation
2000
Stock Market and Ticker/Symbol/Number
not listed because we are private company
Please specify your partnering goal
big pharma, and we are open to other options too.
Funding Status
pre-clinical round of funding
Now raising (In USD)
10 million USD
Headquartner in China
Plan in China
-partnering with Chinese pharmaceutical companies -partnering with Chinese manufacturers especially in the field of peptides and drug manufacturing. -launching our drugs from China (being China Based).
Assets Information 1: Name|Description|Indications|Stage|IP countries
Patents|METHODS AND COMPOSITIONS FOR IDENTIFYING A PEPTIDE HAVING AN INTERMOLECULAR INTERACTION WITH A TARGET OF INTEREST|developing drugs to many illnesses including CANCER AND COVID19|preclinical|not yet
Assets Information 2
patents|THERAPEUTIC MULTI-TARGETING CONSTRUCTS AND USES THEREOF|most types and stages of Cancer|preclinical|not yet
Biotech/Pharma Asset Stage
Investment Focus
private equity but we are open to other options.
Suma Khazmo
Spokesperson and Investment Consultant 
Functionality

AlephBot Israel

AlephBot is developing a new paradigm in healthcare, the procedure monitor.
The solution helps medical teams maximize treatment efficiency during and after medical procedures (e.g., resuscitation, labor, general anesthesia). It provides the team members with valuable real-time information that is adaptive to their actions and to the procedure’s stage, even if they are under pressure or can’t recall procedure steps by heart. AlephBot also automatically documents the medical procedure, which serves for both medical education and medico-legal purposes.

** AlephBot uniqueness **
We capture the human perspective of a procedure by analyzing the relevant info from the on-going structural medical conversation. We add this layer to the data collected from other sources.
Therefore, we gain higher accuracy of the analyzed medical situation, which enables us to identify the procedure stage and provide meaningful info, in real-time.

** Status **
AlephBot is developing its core technology. The company, pre-seed funded, was selected to the DRIVE accelerator at the Technion (Israel institute of Technology), and received grants from the Israel Innovation Authority.
AlephBot cooperates with big and small hospitals from day one. This serves our intention to increase treatment efficiency both in mega-hospitals in big cities and in smaller ones in the periphery and rural areas.

AlephBot is active in its target markets (Germany, France, Italy and the US) and won several national and international (France, Germany, Denmark) events and competitions. The company is still not active in China - an opportunity!

** Next steps **
We are currently looking for seed investment to finalize our core technology development and bring the product to clinical trial stage in two years. Sales are planned in three years, post regulation clearance.

Company Size (Fulltime employees)
Year of foundation
2017
Looking for
Please specify your partnering goal
Fundraising and set the ground for future business in China.
Funding Status
On going seed round
Now raising (In USD)
2,000,000
Headquartner in China
Plan in China
We see great potential in using AlephBot in China, as it could help with the following challenges:* Increase rural medicine level, supporting medical caregivers in rural areas during treatment (caregivers are with limited knowledge, not up-to-date). * Increase treatment efficiency in big hospitals of big cities. These are high-standard hospitals, that use “state of the art” solutions like AlephBot, for better treatment, cost saving and patient satisfaction.
Slides Deck
(pdf, 305.3KB)
Ofer Talmor
Ofer Talmor
CEO and co-founder 
Functionality

Allevetix Medical Israel

Welcome to Allevetix Medical, a global leader in innovative medical technology focusing on treating metabolic diseases such as Type II Diabetes, Obesity, and NASH (Nonalcoholic steatohepatitis).

Allevetix team had developed the NobiX System. It is a non-surgical, fully-reversible, and natural treatment designed to mimic gastric bypass surgery's effects without any need for cuts, ablations, or permanent changes to the patient anatomy. It consists of a safe and non-invasive implant that prevents food contact with a section of the small intestine linked to hormone abnormality in metabolic diseases.
In a matter of months, the NobiX can naturally reduce body weight by 20% and lower HbA1C levels. The effects of the Nobix System begin immediately with patients feeling more energetic and less prone to symptoms of metabolic disease.

The NobiX System allows patients to recover naturally from metabolic diseases by promoting healing and balance in the duodenum through the avoidance of contact and metabolic reactions in this intestinal tract section. The NobiX can be removed and replaced anytime during the patient’s recovery. It is designed to assist patients with balancing metabolic disorders without any necessary changes to their lifestyle.
Company Size (Fulltime employees)
Year of foundation
2017
Funding Status
5.5 m USD were invested at Allevetix to date.
Headquartner in China
Plan in China
Allevetix Medical had started its clinical studies in Europe, and our next goal is to start clinical studies in china as it one of the largest markets for our product. We seek partenters and investors to fund the studies required for submitting the product to the CFDA before commercialization.
Ziv Kalfon
CEO 
Functionality

Carmel Diagnostics ltd. Israel

Carmel Diagnostics is a medtech company who developed an innovative method for measuring Oxidative Stress (OS) of a biological liquid, a recognized biomarker of health and disease and a key diagnostics parameter. This OS parameter is measured by TCL (ThermoChemiLuminescence), an advanced yet simple technology. Carmel’s lead product is Embryo Selection in IVF process. Carmel won the prestigious Phase-2 grant from Horizon2020, planning market launch in H1/2021. It has an experienced, motivated team.

Company Size (Fulltime employees)
Year of foundation
2009
Please specify your partnering goal
Potential licensing
Funding Status
Series A, looking for an investment of 4M USD
Now raising (In USD)
5M
Headquartner in China
Plan in China
We have already registered WFOE in China. Our plans are:Establish Manufacturing site and customer support in ChinaFertissimo distribution in China to improve IVF performancePromote Additional applications in cooperation with Chinese Institutes/Academy/IndustryPromote the use of AI, Bioinformatics and machine learning for optimization and continuous improvement
Medtech Information 1, Device Name|Description|Development Stage|Licensed Countries
Fertissimo TCL Analyzer. CE Mark
Medtech Development Stage
Slides Deck
(pptx, 7.32MB)
Mr Tzali Cnaani
LinkedIn logo CEO 
Functionality

ExoProTher Medical LTD Israel

ExoProTher Medical is an Israeli pre-clinical stage company developing a novel biotherapy for cancer treatment, relevant to all cancers with p53 mutation or inactivation - more than 60% of human cancers. Our technology is unique and disruptive and is fully owned by the company.

The company has been funded by private investors. We are currently working on shaping our next funding round.
Company Size (Fulltime employees)
Year of foundation
2017
Funding Status
Seed round raised in early 2020 from private investors and family offices (international).
Headquartner in China
Plan in China
China is now the second largest pharmaceutical market in the world. China’s oncology market alone represents 37% of all lung cancer, 44% of stomach cancer and 52% of liver cancer patients globally. In addition, Chinese pharma companies are active partners in international development. ExoProTher technology is very relevant and, we believe, very attractive to build such partnership. It may be based on joint development with subsequent licensing of commercial rights for the therapy in China. Another option is establishing a partnership aimed at building a manufacturing facility for our novel therapeutic platform.
Lana Volokh
PhD 
Functionality

iNNOGING Medical Israel

iNNOGING Medical - Remote and offline ultrasound image analysis solution

Ultrasound is a real-time examination and very much operator dependent.
Majority of ultrasound scans are done by technicians and afterwards diagnosed off-line by the expert without the presence of the patient. A major drawback is that the radiologist who determines the diagnoses is not the person who performs the ultrasound scan; hence this workflow might lead to errors and worse to misdiagnoses.
iNNOGING is developing a technology that will provide the radiologists a remote and off-line tool to inspect areas of interest, based on recorded ultrasound scans. Allowing navigation like in real time as if the patient is there with the doctor, while all possible information (any plane) of an organ is visible, even information that was not presented in the original scan.

In addition to the above, we have recently launched an affordable SaaS based Ultrasound Simulator.
Website:
www.innoging.com
Company Size (Fulltime employees)
Year of foundation
2018
Looking for
Funding Status
Seed round done, going to A-Round now
Headquartner in China
Plan in China
We would like to do one of our first clinical trials in China. to aqcuire a CFDA. The Chinese market is growing tremendously and we think it should be the main target for us.
Yehiel Polatov
Co-Founder EVP Business Development 
Functionality

Kitov Pharma Israel

Kitov Pharma (NASDAQ:KTOV) is a clinical stage biopharmaceutical
company advancing first in class oncology therapies. We currently have one FDA
approved drug, Consensi™, and two oncology therapeutic candidates, CM-24 and NT-219:

• CM-24 is a clinical stage mAb targeting CEACAM1, a novel immune checkpoint inhibitor with high potential to treat multiple oncology indications. CEACAM1 is associated with angiogenesis, is an
inter-cellular adhesion regulator and acts as a TIM-3 activator. High CEACAM1 expression is known to be associated with poor disease prognosis in a number of tumor types. Thus, blocking CEACAM1 with CM24 is associated with anti-angiogenic, immune access, and checkpoint release mechanisms. In a phase I
clinical study, CM-24 demonstrated a good safety profile and promising efficacy signals. We are developing CM-24 in a clinical collaboration with Bristol
Myers-Squibb for Phase 1/2 trial combining CM-24 with nivolumab in NSCLC and pancreatic cancer patients expressing high CEACAM1 levels.

• NT-219 is a first-in-class, dual inhibitor small molecule targeting IRS 1/2 and STAT3, two key signal transducers that promote cancer drug resistance. In preclinical studies, NT-219 demonstrated outstanding
efficacy in preventing acquired resistance and reversing tumor resistance when administered as a monotherapy and in combination with various oncology therapies. We are initiating first-in-man clinical trials with NT219, both as monotherapy and in combination with cetuximab (Erbitux™), with plans to expand combination studies in patients with recurrent or metastatic SCCHN cancer during 2020.
Year of foundation
2011
Looking for
Please specify your partnering goal
We are looking for in licensing opportunities in the Oncology drug development field
Headquartner in China
Biotech/Pharma Category
Yael Lahat
Associate Director Business Development 
Functionality

MSL Pharma Israel

MSL Pharma is an early-stage pharma company that performs ideation, analysis and identification of the underlying pathological pathways to determine how to treat diseases. The Company holds exclusive licenses from the Hebrew University & Ben-Gurion University of the Negev. There are data, patents and publications concerning the technologies.

As an early-stage company, in order to reduce overhead costs, we effectively act as the project manager – we plan the assays and subcontract the early development stages to university labs, and the later stages to CROs that specialize in the different fields. The Company monitors the results, determines next steps and fundraises for the next phases of development. We believe that working with leading experts at CROs is critical for success.

The Company has licenses for platform technologies which are progressing to several different projects; as such it is planning to out-license at various stages of development.

Synthesis of cyclic peptides which are peptidomimetics
MSL Pharma has the capability to identify “active regions” of proteins and peptides, to isolate them and to turn them into cyclic peptides which are selective for the desired receptors and stable, thereby preventing off-target activation and adverse effects (see Asset, Table 1).

Drug delivery systems for peptides and other molecules
MSL Pharma has two technologies for drug delivery (see Mode of Delivery, Table 1) that achieve unprecedented bioavailability:
1. Lipophilic prodrug charge masking (LPCM) technology for the oral delivery of peptides. This technology makes a chemical modification in a peptide to be converted to oral delivery, to produce a prodrug of this peptide. This causes it to be absorbed through the intestinal cell and once the prodrug enters the blood stream, it converts back to the original peptide. Typically, the Pgp Efflux system limits the prodrug absorption; we have overcome this with an approved self-assembling PNL (pro-nano liposphere) encapsulation system, itself a self-nanoemulsifying drug delivery system (SNEDDS), which increases prodrug solubility and inhibits the Pgp Efflux system.

2. A novel nanoparticle formulation called AmyloLipid Nanovesicles which is constructed of natural materials and therefore safe ,biodegradable and has an advantage for the delivery of peptides. This technology is used also for the delivery of other molecules, can be used for nose-to-brain, sublingual, transdermal and probably also oral delivery, and can be applied to our assets (Table 1) or existing assets (Table 2).

A novel smart multi-armed linker for targeted drug delivery
Our linker can be used for peptide-drug conjugates (PDCs), antibody-drug conjugates (ADCs) and nanoparticle-drug conjugates (NDCs). Our linker releases the payload (chemotherapeutic drug or fluorescent) only in the tumor cells and can bind up to three payloads (see Table 3). We have demonstrated that using two or three different drug payloads kills the tumor cells more potently and with less drug resistance developing.

Discovery of novel peptides for peptide-drug conjugates
We have technologies to synthesize novel peptides which will bind to receptors overexpressed in certain tumors so that we will be able to use them for synthesizing peptide-drug conjugates (PDCs) to diagnose and treat different tumors. We already have at our disposal peptides that bind to the five different somatostatin receptors (overexpressed in pancreatic, gallbladder, breast, ovary, prostate, melanoma, lymphoma, glioblastoma, colon and non-small-cell lung tumors) and to certain integrin receptors (overexpressed in tumors such as breast, glioblastoma, leukemic cells). 
Company Size (Fulltime employees)
Year of foundation
2012
Please specify your partnering goal
Fundraising Collaborating with a unuversity or reaearch organisation Doing licensing agreements Doing technology ttransfer agreements
Funding Status
Seed
Now raising (In USD)
1,000,000
Headquartner in China
Plan in China
Fundraising Collaborating with a unuversity or reaearch organisation Doing licensing agreements Doing technology ttransfer agreements
Assets Information 1: Name|Description|Indications|Stage|IP countries
backtide G|A Melanocortin 4 & 5 agonist|Obesity, Metabolic Syndrome, Sexual Dysfunction|Seed|
Biotech/Pharma Asset Stage
Slides Deck
(pptx, 3.25MB)
Dr Yarom Cohen
Dr Yarom Cohen
LinkedIn logo CEO 
Functionality

Respinova Ltd. Israel

Respinova has developed a novel non-invasive technology that aims to treat the core of the COPD pathophysiology – small airway collapse.

Respinova's solution uses unique pulses of air pressure generated by a proprietary device called PulseHaler™. ​The small airways have no cartilage structural support and are totally dependent on the tethering forces of the surrounding lung. When these forces are diminished, the small airways collapse and do not permit airflow to the gas-exchanging alveolar zone of the lung. When COPD starts, airways initially reopen on inspiration. Once the disease progresses, the airways open only on deep inspiration, and finally not at all. When the small airways collapse, not only is gas exchange is impaired, but also the cilia clearing mechanism fails, and secretions accumulate to further worsen the situation.

The small airways have little or no smooth muscle in their walls so that neither beta-adrenergic nor muscarinic drugs can open them up, even if the particles manage to be delivered to the small airways.

The PulseHaler™ generates proprietary pressure pulses that travel into the lung which propagate faster inside the airways than in the surrounding parenchyma, thereby creating multiple momentary dilating forces that help gently pry open the collapsed airways. PulseHaler™ also generates positive pressure on exhalation, which helps with airway opening. The pulses also help in smoothing and spreading the mucus lining layer on the airways walls, which assists in airway clearance and reduces the tendency of airways to re-close.

Company Size (Fulltime employees)
Funding Status
Serial B
Now raising (In USD)
$ 10MM
Headquartner in China
Biotech/Pharma Category
Medtech Category
Medtech Information 1, Device Name|Description|Development Stage|Licensed Countries
Pulsehaler | Pulsehaler™ is a novel treatment that uses Dynamic Air Pressure Pulses to re-open closed airways,improve exercise capacity and Quality of Life in COPD patients. | NDA |
Medtech Development Stage
Cliff Ansel
CEO 
Functionality

Selfit Medical Israel

Selfit is a digital therapy startup focusing on the aging population and brain and heart conditions.
The company has developed a therapist robot based on AI and neuroscience with focus on physical and cognitive health.
Please specify your partnering goal
We're looking for partners to test, validate and customized our solution to the Chinese market as well as investors.
Headquartner in China
Shahar Figelman
CEO 
Functionality