Vaccinogen

Vaccinogen Inc
Public
Traded as OTCQB: VGEN
Industry Biotechnology
Founded 2007
Headquarters Baltimore
Key people
Andrew Tussing
(Chairman and Chief Executive Officer)
Michael Hanna
(Founder)
Products OncoVAX
Website www.vaccinogeninc.com

Vaccinogen Inc. is a US biotechnology company developing a potential cancer immunotherapy called OncoVAX, where a patient’s own tumour cells are used as the vaccine, adjuvanted by BCG. This product was evaluated in Phase III in colon cancer in the 1990s and another Phase III study, called ACTIVE, is currently recruiting stage II colon cancer patients. Vaccinogen calls its approach 'Active Specific Immunotherapy' or ASI.

Background

Vaccinogen originated in work done by the company's founder, Dr Michael Hanna, in the late 1970s and early 1980s when he was Director of the National Cancer Institute's Frederick Cancer Research Center in Frederick, Md. Hanna founded a company to develop what became OncoVAX and this was acquired by a company from Seattle called Intracel, but that company but filed for bankruptcy in 2001. Vaccinogen was formed in 2007 to pick up the intellectual property and other assets from Intracel.[1] Dr Ben Carson was Chairman of the company from August 2014[2] until the announcement of his US Presidential bid in May 2015.[3] Carson had previously served on Vaccinogen's Medical Advisory Board.[4]

OncoVAX

OncoVAX is an autologous cancer vaccine, that is, manufactured using the patient’s own tumor cells. The product involves the surgical excision of the tumour and its sterilization and gamma-irradiation in order to render the tumor cells non-dividing. The patient is then administered two injections of these tumor cells mixed with the TICE strain of BCG via intradermal injection. After this the patient receives two more injections of tumour cells but without the BCG. The first three immunizations are delivered weekly approximately a month after surgical resection of the tumor, and the fourth is given six months later.[5] At the present time the product is intended for stage II colon cancer, where tumors have penetrated into the muscles around the colon, but have not visibly spread to lymph nodes of more distant sites.

Development of OncoVAX

Hanna et al. performed three multi-institutional, prospectively randomized, controlled clinical trials of post-resection adjuvant ASI over the two decades to 2001. A meta-analysis of these studies published in the journal Vaccine found 'significant clinical benefits in patients with stage II colon cancer'.[6] Hanna et al. described the 'trials and tribulations' involved in developing OncoVAX in a 2006 paper in the journal Human Vaccines.[7]

* Pilot trial in colon and rectal cancer. Michael Hanna first took his ASI approach into the clinic in a pilot trial at Johns Hopkins Hospital that commenced in 1981. The lead investigator was Dr Herbert C. Hoover Jr., a 'distant nephew' of the 31st US President.[8] The study, which evaluated 80 colon and rectal cancer patients, finally read out data in March 1993 in the Journal of Clinical Oncology. The study found a significant improvement in survival (p=0.02) and disease-free survival (p=0.039) in all eligible colon cancer patients but no benefits in rectal cancer patients.[9]

* Phase III study in stage II and III colon cancer with first generation OncoVAX. This study in 412 patients, which compared ASI+resection vs resection alone, used a treatment regimen of only three weekly intradermal vaccine injections of 107 irradiated autologous tumor cells where the first two injections also contained 107 BCG organisms. After a 7.6-year median follow-up period there were no statistically significant differences in clinical outcomes between the treatment arms however there was a trend towards disease-free survival and overall survival for the ASI patients that got all three doses.[10]

* Phase III trial in colon cancer with second generation OncoVAX. This 254-patient study, which has allowed Vaccinogen to make efficacy claims for its current version of OncoVAX and is called the '8701' study by the company, had its results published in The Lancet in January 1999. In this study the investigators used 107 BCG organisms for the first two doses and added the booster vaccination at six months with 107 irradiated autologous tumour cells. Over a median follow-up period of 5.3 years there was a 44% risk reduction for recurrence for patients that received OncoVAX (p=0.023), but only patients who had stage II disease benefited. For these patients the risk of recurrence was cut by 61%.[11] The cost of the product was subsequently studied by medical technology assessment specialists at the Erasmus University Medical Center in Rotterdam who reported 'impressive health economics benefits' in a paper in Vaccine.[12] In 2012 the investigators revisited the data to see if there was different outcomes for patients with microsatellite instable versus stable colon cancer. In the process they tracked event-free survival for the study population out to 15 years, finding a hazard ratio for the treatment group of 0.62 (p=0.033).[13]

OncoVAX manufacturing

OncoVAX employs a 'centralised' manufacturing process where the patient's tumour sample is shipped to a company-owned cGMP manufacturing facility in the Dutch town of Emmen for processing and then shipped back to the hospital for administration to the patient. In the 8701 study manufacturing was not carried out under cGMP conditions. Subsequent to 8701 a small 15-patient study was carried out with manufacturing taking place under cGMP (ClinicalTrials.gov identifier NCT00016133[14]). This study found that the immunogenicity of OncoVAX was unaffected by the manufacturing process.[15]

Planned clinical study of OncoVAX

Vaccinogen is currently enrolling patients in a confirmatory Phase III clinical study for OncoVAX called ACTIVE that will enroll 550 patients with stage II colon cancer, randomising 1:1 to receive surgery alone or surgery plus OncoVAX (ClinicalTrials.gov identifier NCT02448173[16]). The Primary Endpoint in this study is the Disease-Free Interval.

Vaccinogen plans to conduct a pilot program in parallel with ACTIVE to evaluate OncoVAX in combination with an adjuvant chemotherapy treatment for stage III colon cancer patients.

Human monoclonal antibodies program

In September 2015 Vaccinogen announced an exclusive two-year option with Dublin City University over a high-throughput, multiplex, analysis platform developed in the laboratory of Dr. Paul Leonard called DiCAST (Direct Clone Analysis and Selection Technology).[17] Vaccinogen intends to use DiCAST to screen patient-derived biological samples acquired after those patients have gained anti-cancer immunity in the search for new anti-cancer antibodies.[18]

Vaccinogen stock

Vaccinogen stock is traded OTC in the US. It upgraded its marketplace tier to OTCQB in October 2013.[19] The stock code is VGEN.

Main people

Vaccinogen's Chairman and CEO is Andrew Tussing, a former investment banker who co-founded Vaccinogen with Michael Hanna in 2007. Michael Hanna remains a director. Vaccinogen's COO is Dr Peter Morsing, formerly of AstraZeneca.

Location

Vaccinogen is headquartered in Baltimore on 949 Fell Street near Fell's Point. The company moved there in February 2015 after previously having been located at Frederick, Md.[20] The company also maintains labs in Dublin and its manufacturing facility at Emmen.

References

  1. Dance, Scott (February 27, 2015). "Vaccinogen brings momentum on cancer vaccine research to Baltimore". The Baltimore Sun. Retrieved 26 December 2015.
  2. Dance, Scott (August 25, 2014). "Dr. Ben Carson named chairman of Frederick biotech Vaccinogen". The Baltimore Sun. Retrieved 26 December 2015.
  3. "Vaccinogen Names Co-Founder and CEO Andrew L. Tussing as Chairman of the Board". Vaccinogeninc.com. May 5, 2015. Retrieved 26 December 2015.
  4. "Vaccinogen Names Dr. Benjamin Carson and Dr. Jan B. Vermorken to Medical Advisory Board". Vaccinogen.inc. October 24, 2013. Retrieved 26 December 2015.
  5. Hanna MG (August 1, 2012). "Immunotherapy with autologous tumor cell vaccines for treatment of occult disease in early stage colon cancer". Human Vaccines & Immunotherapeutics. 8 (8): 1156–1160. doi:10.4161/hv.20740. PMC 3551893Freely accessible. PMID 22854664.
  6. Hanna MG Jr; Hoover HC Jr; Vermorken JB; Harris JE; Pinedo HM. (Mar 21, 2001). "Adjuvant active specific immunotherapy of stage II and stage III colon cancer with an autologous tumor cell vaccine: first randomized phase III trials show promise". Vaccine. 19 (17-19): 2576–82. doi:10.1016/s0264-410x(00)00485-0. PMID 11257395.
  7. Hanna MG Jr; Hoover HC Jr; Pinedo HM; Finer M. (July 6, 2006). "Active specific immunotherapy with autologous tumor cell vaccines for stage II colon cancer: logistics, efficacy, safety and immunological pharmacodynamics". Human Vaccines. 2 (4): 185–91. doi:10.4161/hv.2.4.3196. PMID 17012885.
  8. Wlazelek, Ann (September 11, 1995). "Surgeon To Test Vaccine On Local Cancer Patients". The Morning Call. Retrieved 27 December 2015.
  9. Hoover HC Jr; Brandhorst JS; Peters LC; Surdyke MG; Takeshita Y; Madariaga J; Muenz LR; Hanna MG Jr. (Mar 1, 1993). "Adjuvant active specific immunotherapy for human colorectal cancer: 6.5-year median follow-up of a phase III prospectively randomized trial". Journal of Clinical Oncology. 11 (3): 390–9. PMID 8445413.
  10. Harris JE; Ryan L; Hoover HC Jr.; Stuart RK; Oken MM; Benson AB 3rd; Mansour E; Haller DG; Manola J; Hanna MG Jr. (January 1, 2000). "Adjuvant active specific immunotherapy for stage II and III colon cancer with an autologous tumor cell vaccine: Eastern Cooperative Oncology Group Study E5283". Journal of Clinical Oncology. 18 (1): 148–57. PMID 10623705.
  11. Vermorken JB; Claessen AM; van Tinteren H; Gall HE; Ezinga R; Meijer S; Scheper RJ; Meijer CJ; Bloemena E; Ransom JH; Hanna MG Jr; Pinedo HM. (January 30, 1999). "Active specific immunotherapy for stage II and stage III human colon cancer: a randomised trial". Lancet. 353 (9150): 345–50. doi:10.1016/s0140-6736(98)07186-4. PMID 9950438.
  12. Uyl-de Groot CA; Vermorken JB; Hanna MG Jr; Verboom P; Groot MT; Bonsel GJ; Meijer CJ; Pinedo HM. (March 18, 2005). "Immunotherapy with autologous tumor cell-BCG vaccine in patients with colon cancer: a prospective study of medical and economic benefits". Vaccine. 23 (17-18): 2379–87. doi:10.1016/j.vaccine.2005.01.015. PMID 15755632.
  13. de Weger VA; Turksma AW; Voorham QJ; Euler Z; Bril H; van den Eertwegh AJ; Bloemena E; Pinedo HM; Vermorken JB; van Tinteren H; Meijer GA; Hooijberg E. (February 1, 2012). "Clinical effects of adjuvant active specific immunotherapy differ between patients with microsatellite-stable and microsatellite-instable colon cancer". Clinical Cancer Research. 18 (3): 882–9. doi:10.1158/1078-0432.CCR-11-1716. PMID 22156611.
  14. "Vaccine Therapy in Treating Patients With Stage II or Stage III Colon Cancer That Has Been Removed During Surgery". Clinicaltrials.gov. U.S. National Institutes of Health. Retrieved 28 December 2015.
  15. "OncoVAX Cancer Vaccine Clinical Results". Vaccinogeninc.com.
  16. "A Multicenter Study of Active Specific Immunotherapy With OncoVax in Patients With Stage II Colon Cancer". U.S. National Institutes of Health. Retrieved 27 December 2015.
  17. Fitzgerald V; Manning B; O'Donnell B; O'Reilly B; O'Sullivan D; O'Kennedy R; Leonard P. (January 20, 2015). "Exploiting highly ordered subnanoliter volume microcapillaries as microtools for the analysis of antibody producing cells". Analytical Chemistry. 97 (2): 997–1003. doi:10.1021/ac503547j. PMID 25479183.
  18. "Vaccinogen Enhances Patient-Derived Antibody Program with Revolutionary High-Throughput Single Cell Screening and Analysis System". Vaccinogeninc.com. September 9, 2015. Retrieved 27 December 2015.
  19. "Vaccinogen Announces SEC Clearance of Form 10 Registration Statement and Upgrade to OTC.QB Market". Vaccinogeninc.com. October 17, 2013. Retrieved 26 December 2015.
  20. "Vaccinogen Relocates Corporate Headquarters to Baltimore". Vaccinogen.com. February 24, 2015. Retrieved 26 December 2015.
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