Delving into the Latest Updates on Conatumumab with Synapse

Overview

Basic Info

Drug Type

Monoclonal antibody

Synonyms

Conatumumab (USAN/INN), AMG-655

Target

DR5

Action

agonists

Mechanism

DR5 agonists(Tumor necrosis factor receptor superfamily member 10B agonists)

Therapeutic Areas

NeoplasmsImmune System DiseasesDigestive System Disorders+ [5]

Active Indication-

Inactive Indication

Advanced Lung Non-Small Cell CarcinomaAdvanced Malignant Solid NeoplasmCarcinoid Tumor+ [20]

Originator Organization

Amgen, Inc.

Active Organization-

Inactive Organization

ImmunityBio, Inc.

Amgen, Inc.

Takeda Pharmaceutical Co., Ltd.

License Organization

Takeda Pharmaceutical Co., Ltd.

Amgen, Inc.

Drug Highest PhaseDiscontinuedPhase 2

First Approval Date-

Regulation-

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Structure/Sequence

Sequence Code 9532985H

Source: *****

Sequence Code 9532993L

Source: *****

This is a dose escalation study in female subjects with relapsed ovarian cancer (including epithelial ovarian cancer, primary peritoneal cancer, or fallopian tube cancer). Approximately 30 to 40 subjects will be administered a combination of conatumumab and birinapant.
In the initial dose-escalation stage of the study, adult female subjects will receive conatumumab in combination with increasing doses of birinapant in dose-escalation cohorts to determine the MTD of birinapant when administered with a fixed dose of conatumumab.
In safety expansion stage, adult female subjects will receive conatumumab in combination with birinapant at the MTD of the combination.

Start Date01 Nov 2013

Sponsor / Collaborator

TetraLogic Pharmaceuticals Corp.

NCT01327612

/ CompletedPhase 2

A Phase 2 Open Label Extension Study of Conatumumab and AMG 479

The purpose of this protocol is to allow continued treatment with conatumumab and/or ganitumab, with or without chemotherapy, to participants who completed a separate Amgen-sponsored conatumumab or ganitumab study without disease progression whose previous studies were closed.

Start Date03 Mar 2011

Sponsor / Collaborator

Amgen, Inc.

EUCTR2008-005074-12-ES

/ CompletedPhase 1

A Phase 1b/2 Open Label, Dose Escalation Study of AMG 655 in Combination with AMG 479 in Subjects with Advanced, Refractory Solid Tumors. -------------------------------------------------------- Estudio abierto de fase 1b/2 con escalada de dosis de AMG 655 en combinación con AMG 479 en sujetos con tumores sólidos refractarios y avanzados.

Start Date04 Mar 2009

Sponsor / Collaborator-

100 Clinical Results associated with Conatumumab

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100 Translational Medicine associated with Conatumumab

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100 Patents (Medical) associated with Conatumumab

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29

Literatures (Medical) associated with Conatumumab

30 Sep 2025·PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

CRISPR screens identify the ATPase VCP as a druggable therapeutic vulnerability in cholangiocarcinoma

Article

Author: Sun, Zhen ; Beijersbergen, Roderick L. ; Wang, Siying ; Gao, Qiang ; Jin, Haojie ; Lieftink, Cor ; Wang, Liqin ; Qin, Wenxin ; Zheng, Jiaojiao ; Lian, Shuo ; Ji, Shuyi ; Guan, Ming ; Zhu, Huijue ; Wu, Wei ; Wang, Jian ; Jia, Qi ; Shi, Yaoping ; Fan, Zhoulong ; Yang, Wu ; Li, Zhe ; Jansen, Robin A. ; Bernards, René ; Niu, Kongyan ; Deng, Xuan

Cholangiocarcinoma (CCA) remains a lethal malignancy with limited therapeutic options. Through genome-wide CRISPR-Cas9 screening, we identified the adenosine triphosphatase (ATPase) valosin-containing protein (VCP) as a critical dependency in CCA. Compound screens revealed that the VCP inhibitor CB-5339 potently suppresses CCA proliferation in a panel of patient-derived organoids by inducing cellular senescence. It is known that senescent cells persist, and this can contribute to therapy resistance. To address this, we combined CB-5339 with senolytic agents (ABT-263 and conatumumab), which selectively eliminate senescent CCA cells, resulting in enhanced tumor suppression both in vitro and in vivo. Clinical analysis showed that VCP overexpression in CCA patients correlates with poor prognosis. Our study unveils a “one-two punch” strategy, targeting VCP-mediated senescence followed by senolytic clearance, offering a promising therapeutic approach for CCA.

31 Dec 2022·Drug deliveryQ2 · MEDICINE

Combined and targeted drugs delivery system for colorectal cancer treatment: Conatumumab decorated, reactive oxygen species sensitive irinotecan prodrug and quercetin co-loaded nanostructured lipid carriers

Q2 · MEDICINE

ArticleOA

Author: Liu, Youqiang ; Zhao, Liyan ; Liu, Yibing ; Meng, Qingju ; Cui, Haijing ; Zhang, Futong ; Zhang, Hongxin

PURPOSE:

Colorectal cancer (CRC) is the third most frequently diagnosed cancer and this study aimed to develop a conatumumab decorated, irinotecan prodrug and quercetin co-loaded delivery system for combined and targeted colorectal cancer treatment.

METHODS:

A conatumumab (C) decorated, irinotecan prodrug (I-p) and quercetin (Q) co-encapsulated NLC (C I-p/Q NLC) was developed. In vitro and in vivo antitumor efficiency of NLC was evaluated on CRC cells and mice xenograft.

RESULTS:

The results showed that the HT-29 cells uptake of C I-p/Q NLC was over 70%. Reactive oxygen species (ROS) sensitive irinotecan prodrug formulation showed improved drug release ability in hypoxic conditions. C I-p/Q NLC showed significantly higher cytotoxicity than non-decorated NLC, single drug-loaded NLC and free drugs. In vivo studies in a CRC-bearing model corroborated the capability of nanoparticles for the inhibition of cancer, leading to a reduction of tumor growth without systemic toxicity.

CONCLUSION:

The conatumumab decorated, ROS sensitive prodrug contained combination nano-system is a promising platform for CRC therapy.

01 Oct 2020·Advances in therapyQ3 · MEDICINE

Efficacy and Safety of Regorafenib in Combination with Chemotherapy as Second-Line Treatment in Patients with Metastatic Colorectal Cancer: A Network Meta-Analysis and Systematic Literature Review

Q3 · MEDICINE

Review

Author: Cai, Yue ; Xie, Xiaoyu ; Li, Weiwei ; Wu, Zehua ; Hu, Huabin ; Zhang, Jianwei ; Deng, Yanhong ; Ling, Jiayu

INTRODUCTION:

Although various therapies are available for the treatment of metastatic colorectal cancer (mCRC), there is lack of head-to-head evidence. Recent studies have demonstrated the efficacy of chemotherapy in combination with different biological agents including regorafenib in second-line therapy in patients with mCRC. We conducted a network meta-analysis (NMA) to estimate the relative efficacy and safety of regorafenib in combination with chemotherapy compared to other biological agents with chemotherapy combinations.

METHODS:

A literature search was conducted in PubMed, Embase, and Cochrane databases to identify all randomized controlled trials (RCTs) evaluating the efficacy and safety of bevacizumab, regorafenib, panitumumab, cetuximab, ramucirumab, conatumumab, ganitumab, and aflibercept in combination with chemotherapy against chemotherapy alone as second-line setting from inception to 7 February 2019 in patients with mCRC. The survival outcomes were analyzed by the frequentist statistical approach (R software, netmeta package) while the level of individual treatment arms was assessed using the Bayesian method (R software, gemtc package).

RESULTS:

We identified 12 articles involving eight RCTs studies analyzing 6805 patients. The studies compared bevacizumab (3), regorafenib (1), panitumumab (2), cetuximab (3), ramucirumab (1), conatumumab (1), ganitumab (1), and aflibercept (1) against chemotherapy alone as comparator. The progression-free survival (PFS) revealed that regorafenib performed better than aflibercept (HR 0.9631, 95% CI 0.6785-1.367), ganitumab (HR 0.7228, 95% CI 0.3985-1.3109), panitumumab (HR 0.9653, 95% CI 0.6781-1.3742), and ramucirumab (HR 0.9206, 95% CI 0.6504-1.303). Regorafenib performed better than bevacizumab (OR 0.797, 95% CI 0.328-1.88) in terms of tumor response. Safety analysis showed that regorafenib performed better in reducing grade ≥ 3 adverse events (AE) than cetuximab and conatumumab, neutropenia than conatumumab, and fatigue than cetuximab.

CONCLUSIONS:

Regorafenib combined with chemotherapy might be a potential alternative to conventional therapeutic options in second-line treatment of patients with metastatic colorectal cancer and could be considered as the best option for treating patients with KRAS and BRAF mutated mCRC. However future RCTs are needed to confirm these results.

100 Deals associated with Conatumumab

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External Link

KEGG	Wiki	ATC	Drug Bank
D09329	Conatumumab	-	DB11646

R&D Status

10 top R&D records.

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Indication	Highest Phase	Country/Location	Organization	Date
Carcinoid Tumor	Phase 2	United States	Amgen, Inc.	03 Mar 2011
Carcinoid Tumor	Phase 2	Poland	Amgen, Inc.	03 Mar 2011
Carcinoid Tumor	Phase 2	Spain	Amgen, Inc.	03 Mar 2011
Lymphoma	Phase 2	United States	Amgen, Inc.	03 Mar 2011
Lymphoma	Phase 2	Poland	Amgen, Inc.	03 Mar 2011
Lymphoma	Phase 2	Spain	Amgen, Inc.	03 Mar 2011
Advanced Malignant Solid Neoplasm	Phase 2	-	ImmunityBio, Inc.	16 Jan 2009
Colorectal Cancer	Phase 2	-	ImmunityBio, Inc.	16 Jan 2009
Neoplasm Metastasis	Phase 2	-	ImmunityBio, Inc.	16 Jan 2009
Ovarian Cancer	Phase 2	-	ImmunityBio, Inc.	16 Jan 2009

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Clinical Result

Indication

Phase

Evaluation

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Study	Phase	Population	Analyzed Enrollment	Group	Results	Evaluation	Publication Date


NCT00630552 (QUILT-2.019, CTgov)	Phase 1/2	Pancreatic adenocarcinoma \| Metastatic Pancreatic Cancer	138	AMG 655 (Phase 1b AMG 655 3mg/kg)	savfbentqk = jdlhziuikw hzyafzkjer (tpetrfvgrc, kxsxnnriza - powascfxrk) View more	-	17 Oct 2024
				AMG 655 (Phase 1b AMG 655 10mg/kg)	savfbentqk = acgvdgknpm hzyafzkjer (tpetrfvgrc, itxqulrksv - eysdcnwzki) View more
NCT00819169 (CTgov)	Phase 1/2	Sarcoma \| Ovarian Cancer \| Neoplasm Metastasis ... View more	89	AMG 479+AMG 655 (Part 1 Cohort 1)	odpyuxgixk = zsxdqwufgq bmrhqruupj (cxuajgqspb, eeqminnadu - sdqbiwvjlr) View more	-	20 Aug 2024
				AMG 479+AMG 655 (Part 1 Cohort 2)	odpyuxgixk = wwacbeoceu bmrhqruupj (cxuajgqspb, ptfriuunmq - fbahmovsqc) View more
NCT01327612 (CTgov)	Phase 2	Sarcoma \| Carcinoid Tumor \| Neoplasm Metastasis ... View more	12	Ganitumab (20050118: Ganitumab 20 mg/kg)	pqtpmnbosy = sxzswnbrwz qdjabbgpif (rihayhwatr, onqduzpchf - gnwjahhixf) View more	-	21 Feb 2021
				Conatumumab (20050171: Conatumumab 0.45 mg/kg)	pqtpmnbosy = hfeeeizpao qdjabbgpif (rihayhwatr, klcubppavr - anajfxloum) View more
NCT00819169 (Pubmed \| Target Oncol)	Not Applicable	Sarcoma \| Ovarian Cancer \| Neoplasm Metastasis ... View more	78	Ganitumab	sauywfvexm(gqyipntjun) = aukyslyhcp thwhrkjldc (necuzvsubw )	-	01 Mar 2015
NCT00630786 (CTgov)	Phase 1/2	Rectal Cancer \| Colonic Cancer \| Metastatic Colorectal Carcinoma	53	Conatumumab+Panitumumab	jnzuktbxkt = wzsatnkcke blumaggugd (qtzufhuykw, jykgrlotzw - yhuhepdxwv) View more	-	06 Feb 2014
NCT00534027 (Pubmed \| J Thorac Oncol)	Phase 2	Advanced Lung Non-Small Cell Carcinoma First line	172	Paclitaxel-carboplatin + Conatumumab 3 mg/kg	kzhmcxginb(hxmbvmsmlu) = lfnagzkeqc xfkcncwoyc (atafocwghi, 4.1 - 6.3)	Negative	01 Mar 2013
				Paclitaxel-carboplatin + Conatumumab 15 mg/kg	kzhmcxginb(hxmbvmsmlu) = oiijtimpzb xfkcncwoyc (atafocwghi, 3.2 - 6.5)
ASCO2010	Phase 1	Advanced Malignant Solid Neoplasm	9	Conatumumab	thaisalacr(mhmhlntzhx) = occurred in 2 pts jizgsorhzd (jkzpatsdsm ) View more	-	20 May 2010
				AMG 479
ASCO2009	Phase 1	Advanced Lung Non-Small Cell Carcinoma	12	AMG 655 + PC	rdnsgzlqzy(chcvykunxb) = qvysdljwgu smxwlbdzoy (fqltyycqod, 1.5 - 7.0)	-	20 May 2009

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Biosimilar

Competitive landscape of biosimilars in different countries/locations. Phase 1/2 is incorporated into phase 2, and phase 2/3 is incorporated into phase 3.

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