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Rislenemdaz

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Rislenemdaz
Names
IUPAC name
4-Methylbenzyl (3S,4R)-3-fluoro-4-[(2-pyrimidinylamino)methyl]-1-piperidinecarboxylate
Identifiers
3D model (JSmol)
ChemSpider
UNII
  • InChI=1S/C19H23FN4O2/c1-14-3-5-15(6-4-14)13-26-19(25)24-10-7-16(17(20)12-24)11-23-18-21-8-2-9-22-18/h2-6,8-9,16-17H,7,10-13H2,1H3,(H,21,22,23)/t16-,17-/m1/s1
    Key: RECBFDWSXWAXHY-IAGOWNOFSA-N
  • InChI=1/C19H23FN4O2/c1-14-3-5-15(6-4-14)13-26-19(25)24-10-7-16(17(20)12-24)11-23-18-21-8-2-9-22-18/h2-6,8-9,16-17H,7,10-13H2,1H3,(H,21,22,23)/t16-,17-/m1/s1
    Key: RECBFDWSXWAXHY-IAGOWNOFBJ
  • CC1=CC=C(C=C1)COC(=O)N2CC[C@@H]([C@@H](C2)F)CNC3=NC=CC=N3
Properties
C19H23FN4O2
Molar mass 358.417 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

CERC-301 (formerly known as MK-0657) is an orally-active, selective NMDA receptor subunit 2B (NR2B) antagonist which is under development by Cerecor in the United States as an adjunctive therapy for treatment-resistant depression (TRD).[1] In November 2013, phase II clinical trials were initiated,[2] and in the same month, CERC-301 received Fast Track Designation from the Food and Drug Administration for TRD.[3]

A pilot study was published in 2012,[1] and a phase 2 trial was completed in 2014, but was deemed insufficient.[4] A second attempt at a phase 2 trial also found that the drug failed to demonstrate efficacy against depression.[5]

Pharmacology

CERC-301 is a small molecule antagonist of the NMDA receptor. The NMDA receptor is composed of several subunits, but CERC-301 is specific for the GluN2B subunits which are only seen in the spinal cord and forebrain. CERC-301 binds speficically to the GluN2B subunit in order to prevent endogenous glutamate from acting on it. It is considered to be a novel drug for the treatment of MDD and TRD for its immediate onset of efficacy in an oral dosage form.[6] CERC-301 and its active metabolite have been shown to have an onset of action of about 1 hour and half-lives of 12-17h and 21-26h, respectively.[1][7] It has been proven to have a very high binding affinity for its target (K i, 8.1 nmol L−1).[1] This specificity allows CERC-301 to mitigate the symptoms of depression without having many adverse effects due to off target binding.[7]

History

Commercial development

Cerecor acquired the exclusive rights from Merck in 2013 to develop a NMDA receptor antagonist for the treatment of major depressive disorder (MDD). This compound acquired from Merck would eventually become CERC-301.[8] Funds generated through the IPO of Cerecor in 2015 and a common stock purchase agreement with Aspire Capital Fund in 2016 are being used to further develop the molecule.[9][10] Cerecor currently holds three families of patents regarding CERC-301 in the United States as well as several other countries. These patents cover composition of matter, methods of manufacture, methods of use, as well as picture claims to CERC-301 and any pharmaceutical salts of it. These patents will being to expire in 2022 but some will not expire until 2035.[11]

Commercial competitors of the drug include PT00114 from Protagenic, Naurex's NRX-1074, and AV-101 from VistaGen Therapeutics.[12]

Preliminary research

Research into the use of Ketamine to treat MDD had already determined that the drug could have effectiveness in rapidly reducing the symptoms of depression.[13] Unfortunately Ketamine has powerful dissociative effects, leaving patients in a trance-like state after administration and lending itself to recreational abuse. In 2008 a proof of concept study was conducted by Pfizer using the NR2B antagonist Traxoprodil, which proved that drugs similar to Ketamine could be used to treat depressive symptoms without causing the dissociative effect seen in that drug.[14] Traxoprodil was eventually dropped from development due to bioavailability issues and the possibility of it causing QT prolongation.

The first preclinical study of CERC-301 was conducted in 2015 and was primarily geared towards assessing the molecule's safety and pharmacokinetic profile in rats and a small group of men. The study showed that CERC-301 was very orally bioavailable, rapid acting, and that it was safe compared to other similar molecules which had caused neurodegenerative problems in rats.[7] A clinical trial with 135 subjects revealed that CERC-301 does not have any influence on ECG in humans as is seen in Traxoprodil.[15]

Clinical trials

Phase 2

CERC-301 initiated its first phase II randomized double blind clinical trial (NCT01941043) in November, 2013. This study was funded through a $32 million Series B Financing tranche led by venture capital companies such as New Enterprise Associates (NEA), Apple Tree Partners (ATP) and MPM Capital.[16] The trial consisted of 135 patients diagnosed with MDD who were resistant to SSRI/SNRI treatment. The study lasted 28 days and saw patients receiving 8 mg/day doses of CERC-301 in order to see a change in the Hamilton Depression Rating Scale (HDRS) of the patient by day 7, but no significant changes were noted.[15][6]

However, in March 2015, Cerecor announced that the 8 mg dose for the study did not meet the primary objective for the study, although the study showed the safety and tolerance of CERC-301. The company also announced that in a separate study, higher daily doses of drug were able to safely treat patients, indicating that higher doses of drug could be used in future clinical trials.[6]

Cerecor is now conducting a second double blind, randomized, placebo controlled phase 2 clinical trial (NCT02459236) studying the effects of 12 mg/day and 20 mg/day doses of CERC-301 on patients with MDD. Numerous changes were made to the study in order to achieve a great likelihood of success and new top-line data from this study in November 2016.[6] However, the study found that the drug failed to demonstrate efficacy.[5]

See also

References

  1. ^ a b c d Ibrahim L, Diaz Granados N, Jolkovsky L, et al. (August 2012). "A Randomized, placebo-controlled, crossover pilot trial of the oral selective NR2B antagonist MK-0657 in patients with treatment-resistant major depressive disorder". J Clin Psychopharmacol. 32 (4): 551–7. doi:10.1097/JCP.0b013e31825d70d6. PMC 3438886. PMID 22722512.
  2. ^ Yahoo! Finance (2013). "Cerecor Announces Initiation of Phase 2 Study for CERC-301, an Oral Rapid-acting Antidepressant Candidate".
  3. ^ Yahoo! Finance (2013). "Cerecor Receives Fast Track Designation for CERC-301 for the Treatment of Major Depressive Disorder".
  4. ^ "A Randomized, Double-Blind, Placebo-Controlled, Sequential Parallel Study of CERC-301 in the Adjunctive Treatment of Subjects With Severe Depression and Recent Active Suicidal Ideation Despite Antidepressant Treatment". Retrieved 2015-01-04.
  5. ^ a b "Cerecor (CERC) Announces CERC-301 Phase 2 Missed Primary Endpoint in MDD". streetinsider.com.
  6. ^ a b c d "CERC: Results From Phase 2 Clinical Trial of CERC-501 to be Reported in 4Q16…". Retrieved 2016-11-20.
  7. ^ a b c Garner, Rachel; Gopalakrishnan, Shobha; McCauley, John A.; Bednar, Rodney A.; Gaul, Stanley L.; Mosser, Scott D.; Kiss, Laszlo; Lynch, Joseph J.; Patel, Shil (2015-12-23). "Preclinical pharmacology and pharmacokinetics of CERC‐301, a GluN2B‐selective N‐methyl‐D‐aspartate receptor antagonist". Pharmacology Research & Perspectives. 3 (6). doi:10.1002/prp2.198. ISSN 2052-1707. PMC 4777252. PMID 27022470.
  8. ^ Inc, Cerecor. "Cerecor Acquires Rights to NR2B Receptor Antagonist from Merck". www.prnewswire.com. Retrieved 2016-11-20. {{cite web}}: |last= has generic name (help)
  9. ^ "Cerecor raises $26M in IPO - BioCentury.com". www.biocentury.com. Retrieved 2016-11-20.
  10. ^ "Cerecor Enters Into a $15 Million Common Stock Purchase Agreement with Aspire Capital Fund, LLC | Business Wire". www.businesswire.com. Retrieved 2016-11-20.
  11. ^ "CERECOR INC (CERC:NASDAQ CM): Company Description [Page 2] - Bloomberg". www.investing.businessweek.wallst.com. Retrieved 2016-11-20.
  12. ^ "8-K". www.sec.gov. Retrieved 2016-11-20.
  13. ^ Machado-Vieira, Rodrigo; Salvadore, Giacomo; DiazGranados, Nancy; Zarate, Carlos A (2016-11-20). "Ketamine and the next generation of antidepressants with a rapid onset of action". Pharmacology & therapeutics. 123 (2): 143–150. doi:10.1016/j.pharmthera.2009.02.010. ISSN 0163-7258. PMC 2726824. PMID 19397926.
  14. ^ Preskorn, Sheldon H.; Baker, Bryan; Kolluri, Sheela; Menniti, Frank S.; Krams, Michael; Landen, Jaren W. (2008-12-01). "An innovative design to establish proof of concept of the antidepressant effects of the NR2B subunit selective N-methyl-D-aspartate antagonist, CP-101,606, in patients with treatment-refractory major depressive disorder". Journal of Clinical Psychopharmacology. 28 (6): 631–637. doi:10.1097/JCP.0b013e31818a6cea. ISSN 1533-712X. PMID 19011431.
  15. ^ a b Paterson B, Fraser H, Wang C, Marcus R. A Randomized, double-blind, placebo-controlled, sequential parallel study of CERC-301 in the adjunctive treatment of subjects with severe depression and recent active suicidal ideation despite antidepressant treatment. Presented at the 2015 National Network of Depression Centers Annual Conference, November-2015, Ann Arbor, MI, USA
  16. ^ "Cerecor Inc. Closes on Initial Tranche of US$32M Series B Financing | FierceBiotech". www.fiercebiotech.com. Retrieved 2016-11-20.
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