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Exclusive Study! “PFIZER MASKED TOXIC SUBSTANCE inside COVID-19 mRNA VACCINE”. Groundbreaking Discovery on Dangerous ALC-0315 by an Italian Biochemist G. Segalla
by Fabio Giuseppe Carlo Carisio
The Famous Italian Biochemist’s Latest Study on the Pfizer mRNA Vaccine
«ALC-0315, the ionizable cationic lipid enabling the Pfizer vaccine Comirnaty’s LNP platform, is presented in regulatory files as if its metabolic fate were straightforward and well controlled. Our analysis instead identifies a basic, consequential discrepancy that should never survive dossier assembly—let alone review: the hydrolysis product dictated by the ALC-0315 chemicalstructure is 2-hexyldecanoic acid(α-branched), yet key submissions by Pfizer repeatedly invoke the presence of distinct 6-hexyldecanoicisomer (not commercially available, not recognized as an analytical standard in established analytical protocols). This is a material misidentification with direct safety and compliance consequences».
In these few initial lines of his latest disruptive and groundbreaking study, we understand that on this occasion the Italian biochemist Gabriele Segalla has truly outdone himself by revealing a Sherlock Holmes-like instinct in discovering yet another sensational manipulation within the Covid-19 mRNA Comirnaty so-called “vaccine” produced by the New York-based pharmaceutical company Pfizer, perhaps the most used in the world and certainly in the European Union.
Segalla has now published his fourth scientific research paper on Pfizer’s experimental anti-Covid products (which were shown to be ineffective according to a Science study and highly dangerous according to hundreds of other medical articles) and is therefore well acquainted with the nanoparticles, which he immediately defined as “toxic” to humans, with the risk, later supported by dozens of other studies, of causing muscle inflammation, particularly in the heart, such as myocarditis or pericarditis.
A danger that Big Pharma Pfizer and Moderna themselves were then forced to include in the package leaflet by the EMA (European Medicines Agency).
Damage and Health Safety Violations from the Ghost Molecule
Given the highly technical nature of the research published in the American specialist journal International Journal of Vaccine, Theory, Practice, and Research on May 18 (title ALC-0315 Toxic Metabolites: Pharmacokinetic and Regulatory Criticalities in a COVID‑19 “mRNA Vaccine”), we asked out friend PhD Segalla to provide a brief simplified explanation.
«At the heart of the study is a major chemical discrepancy. To track how the vaccine’s protective fat shell (the ALC-0315 lipid) breaks down in pre-clinical tests, official files relied on a “ghost” molecule called 6-hexyldecanoic acid—a substance that does not even exist in international chemical databases. In reality, the vaccine breaks down into a completely different molecule, 2-hexyldecanoic acid, which is globally classified as highly toxic and persistent. The study defines this switch as a “technical falsification” that hid the fact that these toxic ingredients remain trapped inside human cells instead of being safely eliminated».
Indeed, the Italian biochemist so detailed the same issue in his Absttract
«The authentic metabolite, 2-hexyldecanoic acid, concealed by Pfizer and disguised as 6-hexyldecanoic acid, carries an H410 classification (very toxic to aquatic life with long-lasting effects), while the “phantom”6-hexyl isomer is lacking any hazardous classification and presented as theoretically more degradable. In a CMA (Conditional Marketing Authorization) supporting pivotal preclinical study, substituting 2-hexyl with an unclassified 6-hexyl isomer materially compromises the clearance account, traceability, and any defensible claim of GLP (Good Laboratory Pratice) grade validation for Pfizer’s vaccine».
Dr. Segalla’s research demonstrates that this hidden molecule triggers a domino effect of severe biological damage:
- Energy Blackout: It shuts down the cell’s power plants (mitochondria), draining the energy needed to repair our DNA.
- Cell Defense Breach: Another byproduct acts like a harsh chemical detergent, stripping away the protective shield around the cell’s nucleus and risking genomic instability.
- Protein Factory Sabotage: It causes the cell’s internal factories (ribosomes) to glitch. This “factory error” forces the body to produce deformed, unnatural proteins, which can cause the immune system to misfire and attack its own tissues, potentially leading to heart inflammation like myocarditis and pericarditis.
The expert researcher, in an exclusive interview with the editor of Gospa News (currently only in Italian), highlighted the multiple public health violations resulting from his discovery making the request to withdraw the authorization for the Comirnaty mRNA vaccine inevitable.
The Interview with PhD Segalla by Gospa News
We are sorry bot at the monent the Interview in the Video below is in Italian only but we are working to translate it to add subtitles in English
A Discrepancy, Undetected by Drug Regulators, That Would Have Blocked the Authorization of Pfizer’s Gene Serum
This discrepancy is not a technical detail; it directly affects analytical validation, standard traceability, toxicological assessment, metabolic clearance, and the entire regulatory framework.
That is, as Segalla explains in the video interview, if the reporting of the metabolite produced by ALC-0315 in the human body had been correct, the Comirnaty “vaccine” would never have received approval from the competent bodies responsible for overseeing the drug authorization process (FDA, EMA, AIFA, Ministry of Health, etc.).
Not only that. The Italian biochemist is surprised that the EMA failed to detect this enormous discrepancy, but in a previous study, Segalla himself had demonstrated that the EMA could not have been unaware of the toxicity of these nanoparticles, which are highly inflammatory to the muscular system (another recent study has reiterated this) and also potentially carcinogenic.
More Dangers from Trialkanolamine, a Destabilizer of the “Cellular DNA Safe”
«The second breakdown product (a trialkanolamine, pKa ≈ 9.6) is liable to lysosomal sequestration, there by impeding clearance; however, the Pfizer dossier offers only limited substantiation of its disposition. Critically, the pharmacokinetic dataset does not adequately account for dose biodistribution and is predicated on insufficiently documented—or omitted—testing standards. Given the scale of exposure (billionsof subjects) and the potential oncological and cardiological consequences placed on these Pharmacokinetic criticalities, these omissions are not merely unfortunate; they are utterly unacceptable».
As we can read in the Segalla’s new study Abstract, the second critical front concerns trialkanolamine, another degradation product of ALC-0315, described as a cationic molecule capable of remaining trapped in lysosomes, altering cellular autophagy, promoting phospholipidosis, oxidative stress, mitochondrial dysfunction and destabilization of cellular and nuclear membranes.
In the interview, Segalla clarifies that this substance acts as “a degreaser capable of damaging the cellular DNA vault,” causing unpredictable genomic damage, which has also been confirmed by a recent, disconcerting American study, and potentially leading to turbo-cancer consequences.
A Call to Action and Immediate Recall for “Serious Safety Failure to Perform ”
The study argues that regulatory agencies, including the EMA, failed to spot these discrepancies, invalidating the vaccine’s conditional approval.
“This is not just a minor technicality,” states Dr. Segalla. “The lack of traceability masked a critical bioaccumulation risk, exposing the public to unmonitored chronic effects.” Invoking the precautionary principle and Article 10 of the Nuremberg Code, the study demands an immediate revocation of the vaccine’s marketing authorization and calls for an urgent international review of mRNA nanotechnology safety.
«Accordingly, we call for an independent, methodologically transparent and fully auditable re-assessment of ALC 0315 metabolism and clearance, and for all regulatory decisions concerning the Comirnaty medicinal product be reconsidered in view of what appears to amount to a grave and consequential omission in verification procedures» sentenced the Abstract of the study too.
The study links these critical issues to potential long-term biological consequences, including interference with genomic stability, the inflammatory response, cardiaological mechanisms, and protein translation processes, such as ribosomal stalling and frameshifting.
Regarding these issues, Gospa News has published countless disturbing studies on the potential harms of mRNA vaccines, from February 2021 until a week ago. This is precisely why our online news outlet has been banned or blocked from all social media (even Telegram, where we have been repeatedly suspended).
Fabio Giuseppe Carlo Carisio – Founder and Director of Gospa News
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Full pdf: https://ijvtpr.com/index.php/IJVTPR/article/view/128/437
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