OrigAMI-1
amivantamab; amivantamab plus mFOLFOX6; amivantamab plus FOLFIRI in RAS/BRAF wild-type metastatic colorectal cancer
OrigAMI-1 asks whether amivantamab, alone or with chemotherapy, can produce tumor responses with acceptable safety in advanced or metastatic colorectal cancer. Commentary spans X and Bluesky posts, podcasts and YouTube discussions, with medical oncologists among the speakers. The discussion turns on how far enthusiasm for amivantamab in right-sided or previously anti-EGFR-treated disease should extend, when EGFR-directed rechallenge is appropriate, and whether earlier-line chemotherapy combinations will gain phase 3 validation.
- NCT05379595 ↗
- v1.0.0 · edition 1
- updated Oct 31, 2026
- Standard
11 findings, and what sits behind each
01. Right-sided activity supports a trial discussion, not an unconditional treatment recommendation
7 statements · 6 passages · 1 sources · 3 named voices
Counterview: recorded · Limitations recorded: 2. Feeds the Medical Affairs question.
Draws on: Population and setting, Safety and tolerability.
02. Activity after anti-EGFR exposure and in right-sided disease drives enthusiasm, with important evidence limits
18 statements · 16 passages · 7 sources · 6 named voices
Counterview: recorded · Limitations recorded: 3. Feeds the Medical Affairs question.
Draws on: Primary endpoint: Cohorts A, B, and C: Objective Response Rate (ORR), Secondary endpoints, Design and conduct, Safety and tolerability, Population and setting, Primary endpoint: Cohorts D and E: Number of Participants with Adverse Events (AE), The comparison.
03. Rechallenge interest depends on interval, prior response and molecular reversion—not elapsed time alone
14 statements · 9 passages · 6 sources · 4 named voices
Counterview: recorded · Limitations recorded: 3. Feeds the Medical Affairs question.
04. ctDNA-guided selection is constrained by access to both testing and treatment
8 statements · 2 passages · 1 sources · 1 named voices
Counterview: none recorded · Limitations recorded: 3. Feeds the Medical Affairs question.
05. Molecular characterization may refine sidedness-based selection, but does not erase treatment-line distinctions
23 statements · 16 passages · 3 sources · 4 named voices
Counterview: recorded · Limitations recorded: 3. Feeds the Medical Affairs question.
Draws on: Design and conduct.
06. Mechanistic and correlative interest remains hypothesis-led
19 statements · 16 passages · 8 sources · 5 named voices
Counterview: recorded · Limitations recorded: 3. Feeds the Medical Affairs question.
Draws on: Design and conduct.
07. Manageable toxicity is not negligible toxicity, and the formulation question remains setting-specific
11 statements · 11 passages · 9 sources · 8 named voices
Counterview: recorded · Limitations recorded: 3. Feeds the Medical Affairs question.
Draws on: Safety and tolerability, Secondary endpoints, Primary endpoint: Cohorts A, B, and C: Objective Response Rate (ORR), Primary endpoint: Cohorts D and E: Number of Participants with Adverse Events (AE), Population and setting.
08. Earlier-line combination signals generate interest without establishing chemotherapy replacement
8 statements · 8 passages · 6 sources · 7 named voices
Counterview: recorded · Limitations recorded: 4. Feeds the Medical Affairs question.
Draws on: Secondary endpoints, Primary endpoint: Cohorts D and E: Number of Participants with Adverse Events (AE), The comparison, Safety and tolerability.
09. Phase 3 development is anticipated validation, not validation already achieved
22 statements · 15 passages · 10 sources · 7 named voices
Counterview: recorded · Limitations recorded: 4. Feeds the Medical Affairs question.
Draws on: Design and conduct, Population and setting, The comparison.
10. Alternative bispecifics broaden the development question, with tolerability and small datasets limiting comparison
10 statements · 9 passages · 1 sources · 2 named voices
Counterview: recorded · Limitations recorded: 3. Feeds the Medical Affairs question.
Draws on: Safety and tolerability, Design and conduct.
11. Strong public reactions and compassionate-use applications do not establish treatment delivery or consensus
9 statements · 8 passages · 8 sources · 7 named voices
Counterview: none recorded · Limitations recorded: 3. Feeds the Medical Affairs question.
Draws on: Primary endpoint: Cohorts A, B, and C: Objective Response Rate (ORR).
Counts overlap, since one statement can back several findings. They show what the report kept, not how many clinicians agree. The full report includes the interpretations and source links.
Select a finding to see what the full report holds for it: how many verified HCP statements and of what kind, the passages behind them, the sources and voices, and the counterview and limits it records. Select a part of the trial to see which findings draw on it.
- Finding 1 of 11
Right-sided activity supports a trial discussion, not an unconditional treatment recommendation
- statements
- 7
- passages
- 6
- sources
- 1
- named voices
- 3
What the statements areViews 4Questions and uncertainty 1Clinical experience 1Comparisons 0Restated results and context 1How passages are usedSupporting a statement 8Giving context 4Recorded with the finding- Counterview: recorded
- Limitations: 2
- Feeds the Medical Affairs question
- 1 podcast or video
Draws on: Population and setting, Safety and tolerability.
In the full report: the interpretation in full, all 7 statements cited to source and date, and the 1 source linked where public.
Thicker lines mean more shared statements. A finding without a line goes beyond the registered design. Counts overlap, since one statement can back several findings, and they show what the report kept, not how many clinicians agree.
The full OrigAMI-1 report gives each finding its interpretation, the attributed views behind it, counterviews, limits and the verified HCP statements, each linked to the original. Get a complete report free to see what you get.
What comparative benefit, molecular selection, treatment-free interval, tolerability and feasible access pathway would justify moving from trial interest to a routine-care role?
Raised by the leading finding. The report shows what clinicians said and the sources behind it; it does not settle the question.
By the numbers
free- 70HCP commentary sources screened
- 34sources cited by verified HCP statements
- 23named in screened sources
- 23voices cited in the report
- 18cited voices matched to verified clinician profiles
Also in the sources: 7 organizational or shared accounts, not counted as people.
- 180verified statements, each linked to its source
- 102of them from speakers with a confirmed clinical role
- 11findings
Screened sources were retrieved for this trial. Cited sources back at least one verified statement and include primary sources used for context. No count estimates how many clinicians hold a view. Size (Standard) is set by the 180 verified statements. Statements from sponsors, hosts and organisations are labelled and count apart from identified clinicians. A confirmed clinical role is one verified by the NPI registry or by the person's own institution's staff page; a role a source only states is not counted.
What's inside
free| Section | Items | Access |
|---|---|---|
| Findings with interpretation, counterviews and limits | 11 | Titles free |
| Detailed analysis | 13 sections | Paid |
| Verified statements with short source quotes and links | 180 | Paid |
| Trial aspects mapped | 23 | Free |
| Sources with links | 34 | Counts free |
| Speaker attribution for cited voices | 23 | Paid |
Trial aspects
16 discussed · 7 no commentary · 0 incomplete| Aspect | Statements | Sources |
|---|---|---|
| Primary endpoint: Cohorts A, B, and C: Objective Response Rate (ORR) | 16 | 11 |
| Primary endpoint: Cohorts Ph1b-D and Ph1b-E: Number of Participants with Dose-limiting Toxicity (DLT)no commentary found | 0 | 0 |
| Primary endpoint: Cohorts Ph1b-D and Ph1b-E: Number of Participants with DLT by Severityno commentary found | 0 | 0 |
| Primary endpoint: Cohorts D and E: Number of Participants with Adverse Events (AE) | 3 | 3 |
| Primary endpoint: Cohorts D and E: Number of Participants with Laboratory Values Abnormalitiesno commentary found | 0 | 0 |
| Primary endpoint: Cohorts D and E: Number of Participants with Vital Signs Abnormalitiesno commentary found | 0 | 0 |
| Primary endpoint: Cohorts F: Number of Participants with Adverse Events (AE)no commentary found | 0 | 0 |
| Primary endpoint: Cohorts F: Number of Participants with Laboratory Values Abnormalitiesno commentary found | 0 | 0 |
| Primary endpoint: Cohorts F: Number of Participants with Vital Signs Abnormalitiesno commentary found | 0 | 0 |
| Secondary endpoints | 14 | 11 |
| Population and setting | 13 | 9 |
| The comparison | 7 | 7 |
| Safety and tolerability | 12 | 11 |
| Design and conduct | 12 | 7 |
| Right-sided second-line trial consideration and reasons for caution | 8 | 1 |
| EGFR rechallenge biology, interval and intervening treatment | 12 | 5 |
| ctDNA implementation, funding and unequal access | 8 | 1 |
| Conventional anti-EGFR alternatives, sidedness and molecular work-up | 22 | 3 |
| Resistance mechanisms and exploratory correlative markers | 18 | 7 |
| Earlier-line combination development and randomized comparator questions | 29 | 16 |
| Alternative bispecific strategies and preserving useful chemotherapy | 9 | 1 |
| Subcutaneous formulation in the CRC setting | 2 | 1 |
| Access seeking, public amplification and patient-facing participation descriptions | 13 | 9 |
An aspect marked incomplete is a question the public commentary did not let us answer. We show it rather than hide it.
Sources
free| Channel | Screened | Cited | |
|---|---|---|---|
| X threads | 55 | 22 | |
| YouTube | 8 | 8 | |
| Podcasts | 3 | 3 | |
| Bluesky threads | 4 | 0 | |
| Primary sources, cited for context, not screened | |||
| Publications | not screened | 1 | |
max 23 / quarter
- Screened window
- Jul 5, 2023 → Sep 18, 2026
- Cited window
- Sep 15, 2023 → Aug 13, 2026
- Retrieved
- Oct 31, 2026
The trial
from ClinicalTrials.gov- Title
- A Phase 1b/2, Open-Label Study of Amivantamab Monotherapy and in Addition to Standard-of-Care Chemotherapy in Participants With Advanced or Metastatic Colorectal Cancer
- Registry
- NCT05379595
- Study IDs
- CR109215 · 61186372GIC2002 (Janssen Research & Development, LLC) · 2021-006629-23 · 2023-506517-22-00 (EUCT number)
- Sponsor
- Janssen Research & Development, LLC
- Design
- Phase 1/Phase 2 · Interventional, non randomized, parallel
- Status
- Recruiting
- Enrollment
- 225 estimated
- Registered
- 2022-05-18
- Start
- 2022-07-29 actual
- Primary completion
- 2027-04-27 estimated
- Primary endpoint
- Cohorts A, B, and C: Objective Response Rate (ORR)
- Interventions
- 6 registered
Scope and limits
freeThis report does not judge efficacy, estimate HCP prevalence or consensus or give treatment advice.
- Discussion that does not name the trial may be missing from this edition.
- Not yet captured in this edition: a view on pembrolizumab versus chemotherapy and crossover-related interpretation in MSI-high advanced or metastatic colorectal cancer.
- Not yet captured in this edition: a view on orthogonal confirmation of mismatch-repair testing to avoid misclassification before metastatic colorectal cancer treatment.
- Not yet captured in this edition: a view on alternative later-line treatment sequences guided by patient goals and discussion of risks and benefits.
- Not yet captured in this edition: a view on dual-method mismatch-repair testing to avoid misclassification when selecting treatment for metastatic colorectal cancer.
- Not yet captured in this edition: a view on confirming mismatch-repair immunohistochemistry with an orthogonal method to avoid misclassification before systemic-treatment selection.
- Some passages in the sources used in this report were not fully assessed for clinician views, so a view there may be missing from this edition.
- 178 statements in the sources reviewed for this edition are about other patients or topics, or only mention the trial, and are not counted.
- Further source limits: discussion that describes the trial without naming it may be incomplete; some discussion that describes the trial without naming it may be missing; sources about other trials are not included.
- Discussion coverage is incomplete. References that do not use the trial's recognized names or identifier, including different spellings, may be missing.
- Some portions of longer discussions were not fully assessed for clinician views; potentially relevant testing and treatment-sequencing positions may therefore be absent. The referral discussion is not exhaustive: not every alternative trial and its prior-treatment conditions is described here.
- Multiple podcast/video versions and reposts repeat material. Source counts cannot be interpreted as independent-HCP counts or consensus.
- Some remarks cannot be assigned to a named speaker. A participant list, title, profile or publication authorship does not resolve who spoke those passages.
- Some named public authors do not have an established clinical role in the sources reviewed. Organizational summaries and source-described roles or trial involvement are not independent confirmation of clinical credentials or independence.
- The early-phase monotherapy population was highly selected, with small cohorts, early enrollment closure in two cohorts and possible survivor bias in the interval analysis. These constraints limit generalization and comparative interpretation.
- Different reports concern monotherapy, chemotherapy combinations, different cohorts and different follow-up. Their response, durability and safety descriptions should not be pooled.
- A speaker's right-sided CRC post and another speaker's future-studies interview do not name OrigAMI-1 and are treated as setting or development context, not as this trial's results.
- Some source descriptions of treatment allocation, comparators and eligibility are not corroborated by the cited primary statements. They are preserved as what was said, not as validated study methods.
- A full protocol and complete colorectal-cancer regulatory assessment were not available. This report does not establish exact current eligibility, entitlement to access or approved CRC use.
How reports are built and checked: Methods.
Editions and corrections
freeLast checked for new commentary Oct 31, 2026. A new or changed finding gets a new version number; added evidence alone is a smaller update. No corrections.
Cite this report
Erudio Health. OrigAMI-1 (NCT05379595): HCP commentary report. Edition 1, v1.0.0. Accepted Oct 31, 2026. https://www.erudio.com/reports/origami-1-nct05379595
For your AI agent
Paste this into ChatGPT, Claude, Microsoft Copilot or your own agent. It previews this report through the free Erudio MCP server, tells you whether it answers your question, and orders it if you ask. Some agents ask you to confirm pasted instructions before acting; that is expected.
Help me decide whether to buy the Erudio report "OrigAMI-1" (NCT05379595), and buy it for me if I ask. Erudio reports cover what clinicians say in public about one clinical trial, with every verified statement linked to its source.
1. Use the free Erudio MCP server at https://mcp.erudio.com/free; it needs no sign-in. Nothing needs installing: if it is not connected in this app and you can make HTTP requests, call it directly with JSON-RPC POSTs to that URL (initialize, then tools/call), sending "Accept: application/json, text/event-stream". Call get_report_card with slug "origami-1-05379595". If you cannot make requests, read https://www.erudio.com/reports/origami-1-nct05379595.md instead.
2. In a few lines, tell me what the report covers: its findings, its verified statements and sources, its evidence window, what it leaves out, and the price of each product (offer). Then ask what I need it for, and say plainly whether this report answers it.
3. If I want it, ask for my work email and the product: the current edition, or 3, 6 or 12 months of weekly updates. Call create_order with report "NCT05379595", that product and email, then show me the quote and the checkout_url to pay by card. If you have a payment client for HTTP 402 payments and I agree, you can pay the pay_url instead. Nothing is charged until one is paid.
4. Once it is paid, call get_order with the status_url: it returns my license key. Then use the Erudio MCP server at https://mcp.erudio.com/mcp with the header "Authorization: Bearer <key>". Call read_report with report_id erudio-nct05379595 and sections ["all"], and summarize the findings for me with their sources. The full report is large (about 500 KB): save the response to a file and work from it rather than printing it. If you cannot, read sections ["narratives"] first, the executive summary and analysis.
When you tell me what clinicians said, give each view as theirs, with its source. Counts are the sources the report kept, not the share of clinicians who agree. Reports are not medical advice.
Keep the key private to my organization.Or read the record directly: JSON, Markdown or MCP
curl https://www.erudio.com/reports/origami-1-nct05379595.json
curl https://www.erudio.com/reports/origami-1-nct05379595.md
# MCP, no sign-in (https://mcp.erudio.com/free)
get_report_card({ "slug": "origami-1-05379595" })release e9c692bac11f927dc671a72d418081f57411561a0bc003fe259b9757a302a051